Thermochemistry

Preparation for General Chemistry · Dr. Karmach

Dr. Karmach

By the end of this unit, you can…

  • Tell kinetic from potential energy and convert energy among joules, calories, kilojoules, and food Calories
  • Classify a process as exothermic or endothermic from the sign of ΔH, a heat term in the equation, or what is observed
  • Use q = m·c·ΔT to find heat, mass, specific heat, or temperature change, and compare how specific heats set the temperature response to the same heat
  • Apply heat lost = heat gained in a coffee-cup calorimeter to find the heat change of a metal, its specific heat, or the heat of a reaction in solution
  • Find the energy content of a food from the water's temperature rise in a bomb calorimeter, in kJ and Calories per gram
  • Write a thermochemical equation and use ΔH as a conversion factor for moles or grams of any substance in it
Dr. Karmach

Today's route 🗺️

  1. Energy & Its Units
  2. Exothermic & Endothermic
  3. Specific Heat & q = mcΔT
  4. Comparing Specific Heats
  5. Calorimetry
  6. Thermochemical Equations
Dr. Karmach

1 · Energy & Its Units

Tell kinetic from potential energy and heat from temperature, and convert any amount of energy among joules, calories, kilojoules, and food Calories.

Dr. Karmach

Same snack, two labels

The same snack bar sells in two countries. One label lists 230 Calories; the other lists 960 kJ. Both describe the same energy, counted in different units.

Dr. Karmach

Energy is never created or destroyed

Energy is the capacity to transfer heat or to do work. A process moves energy from one place to another or changes its form. The total amount never changes.

energy leaving one place = energy arriving in another
the total is fixed, so an amount of energy can be counted, like mass
Dr. Karmach

Kinetic and potential energy

Kinetic energy is energy of motion. Potential energy is energy stored by position or arrangement. Fuels hold chemical potential energy: stored in the arrangement of atoms, released when a reaction rearranges them.

Dr. Karmach

Two ways energy transfers: heat and work

Energy transfers between things in exactly two ways. Heat (q) is transfer driven by a temperature difference. Work (w) is transfer by a force moving something.

heat (q): hot pan → cool water
energy flows because the temperatures differ
work (w): expanding gas pushes a piston
energy moves because a force acts through a distance
Dr. Karmach

Temperature is not heat

Temperature measures the average kinetic energy of the particles: an intensity. Heat is an amount of energy in transfer. More sample means more energy at the same temperature.

a cup and a bathtub, both at 40 °C
same temperature, yet the tub transfers far more heat as it cools
Dr. Karmach

The units of energy

The SI unit is the joule (J). 1 cal = 4.184 J, exactly. The food Calorie has a capital C: 1 Cal = 1 kcal = 1000 cal. Each equality is an ordinary conversion factor.

Dr. Karmach

The method

  1. Write the given: number and unit.
  2. Plan the route: given unit → wanted unit. Read a capital C as 1000 cal.
  3. Chain the factors so each unit cancels.
  4. Sense-check the size and the surviving unit.
Dr. Karmach

Worked example 1: calories to joules

Step 1 · Write the given

1 cal = 4.184 J
given: 175 cal · wanted: J

A single-use hand warmer releases 175 cal of heat as the iron inside it rusts. Express the energy in joules.

Dr. Karmach

Worked example 1: solution

1 cal = 4.184 J
given: 175 cal · wanted: J

Step 2 · Plan the route

One arrow links the units: cal → J. One conversion factor is needed.

Dr. Karmach

Worked example 1: solution

1 cal = 4.184 J
given: 175 cal · wanted: J
Step 2 · Plan the route Step 3 · Chain the factors so each unit cancels

The factor takes cal in the denominator, so cal cancels and J survives:

175 cal × 4.184 J1 cal = 732 J
Dr. Karmach

Worked example 1: solution

1 cal = 4.184 J
given: 175 cal · wanted: J
Step 2 · Plan the route Step 3 · Chain the factors so each unit cancels
175 cal × 4.184 J1 cal = 732 J
Step 4 · Sense-check
A joule is smaller than a calorie, so the count in joules must be larger: 175 → 732. The heat itself is unchanged. ✓
Dr. Karmach

Worked example 1: the route on the map

1 cal = 4.184 J
given: 175 cal · found: 732 J

The units cal and J share one edge. One equality gives one conversion factor. ✓
Dr. Karmach

Worked example 2: kilojoules to calories

Step 1 · Write the given

1 kJ = 1000 J · 1 cal = 4.184 J
given: 2.50 kJ · wanted: cal

An instant cold pack absorbs 2.50 kJ of heat from the skin it touches. Express the energy in calories.

Dr. Karmach

Worked example 2: solution

1 kJ = 1000 J · 1 cal = 4.184 J
given: 2.50 kJ · wanted: cal · plan: kJ → J → cal

Step 2 · Plan the route

No single equality links kJ to cal. The route runs through the joule: kJ → J → cal. Two conversion factors are needed.

Dr. Karmach

Worked example 2: solution

1 kJ = 1000 J · 1 cal = 4.184 J
given: 2.50 kJ · wanted: cal · plan: kJ → J → cal
Step 2 · Plan the route Step 3 · Chain the factors so each unit cancels

The prefix factor cancels kJ; the calorie factor takes J in the denominator:

2.50 kJ × 1000 J1 kJ × 1 cal4.184 J = 598 cal
Dr. Karmach

Worked example 2: solution

1 kJ = 1000 J · 1 cal = 4.184 J
given: 2.50 kJ · wanted: cal · plan: kJ → J → cal
Step 2 · Plan the route Step 3 · Chain the factors so each unit cancels
2.50 kJ × 1000 J1 kJ × 1 cal4.184 J = 598 cal
Step 4 · Sense-check
One calorie holds 4.184 J, so 2500 J make fewer calories than joules: 598. The pack absorbs the same heat under either name. ✓
Dr. Karmach

Worked example 2: the route on the map

1 kJ = 1000 J · 1 cal = 4.184 J
given: 2.50 kJ · found: 598 cal

No edge joins kJ to cal. The route takes two edges through the joule: two conversion factors. ✓
Dr. Karmach

Your turn: calories to kilojoules

1 cal = 4.184 J · 1 kJ = 1000 J
given: 7.10 × 10³ cal · wanted: kJ · plan: cal → J → kJ

Burning one gram of ethanol releases 7.10 × 10³ cal.

7.10 × 10³ cal × 4.184 J1 cal × kJ J = kJ

Fill the second factor from 1 kJ = 1000 J, then compute.

Dr. Karmach

Your turn: calories to kilojoules

1 cal = 4.184 J · 1 kJ = 1000 J
given: 7.10 × 10³ cal · wanted: kJ · plan: cal → J → kJ

Burning one gram of ethanol releases 7.10 × 10³ cal.

7.10 × 10³ cal × 4.184 J1 cal × kJ J = kJ

Fill the second factor from 1 kJ = 1000 J, then compute.

7.10 × 10³ cal × 4.184 J1 cal × 1 kJ1000 J = 29.7 kJ
Dr. Karmach

Where this goes wrong

Writing the 4.184 factor upside down. 175 cal × (1 cal / 4.184 J) = 41.8 cal²/J. No unit cancels, and the answer is not in joules. The factor that cancels cal gives 732 J.
Stopping at joules. The plan cal → J → kJ has two arrows. Stopping after one leaves 2.97 × 10⁴ J: joules, not the wanted kilojoules. The chain ends at 29.7 kJ.
Reading temperature as an amount of energy. A cup of tea and a bathtub of water can both read 40 °C. The temperatures match; the tub holds far more energy. Temperature is an intensity; heat is an amount.
Dr. Karmach

Practice 1

1 cal = 4.184 J
given: 1.10 × 10³ J · wanted: cal

A burning kitchen match releases 1.10 × 10³ J of heat. How many calories is that?

  1. 1.10 × 10³
  2. 0.263
  3. 263
  4. 4.60 × 10³
Dr. Karmach

Practice 1 · answer: C

1 cal = 4.184 J
given: 1.10 × 10³ J · plan: J → cal
1.10 × 10³ J × 1 cal4.184 J = 263 cal (answer C)

D flipped the 4.184 factor: 1.10 × 10³ × 4.184 = 4.60 × 10³, and no unit cancels. A skipped the conversion: 1.10 × 10³ is still the count of joules. B also divided by 1000, as if the wanted unit were the food Calorie: 1.10 × 10³ / 4.184 / 1000 = 0.263.

Each calorie holds 4.184 J, so the count in calories is smaller than the count in joules: 1.10 × 10³ → 263. ✓
Dr. Karmach

Practice 2

1 kJ = 1000 J · 1 cal = 4.184 J
given: 6.20 kJ · wanted: cal

Dissolving calcium chloride in a beaker of water releases 6.20 kJ of heat. How many calories is that?

  1. 2.59 × 10⁴
  2. 1.48 × 10³
  3. 6.20 × 10³
  4. 1.48
Dr. Karmach

Practice 2 · answer: B

1 kJ = 1000 J · 1 cal = 4.184 J
given: 6.20 kJ · plan: kJ → J → cal
6.20 kJ × 1000 J1 kJ × 1 cal4.184 J = 1.48 × 10³ cal (answer B)

A flipped the 4.184 factor: 6.20 × 10³ × 4.184 = 2.59 × 10⁴, and no unit cancels. C stopped after the prefix factor: 6.20 × 1000 = 6.20 × 10³, a count of joules, not calories. D treated kilojoules as joules: 6.20 / 4.184 = 1.48, a thousand times too small.

Each calorie holds 4.184 J, so 6.20 × 10³ J make fewer calories than joules: 1.48 × 10³. ✓
Dr. Karmach

Worked example 3: the food Calorie

Step 1 · Write the given

1 Cal = 1000 cal · 1 cal = 4.184 J · 1 kJ = 1000 J
given: 230 Cal · wanted: kJ

A snack bar's label lists 230 Calories; the same bar abroad is labeled 960 kJ. Express 230 Cal in kilojoules.

A common first attempt treats 230 Calories as 230 calories. Test it.

Dr. Karmach

Worked example 3: solution

1 Cal = 1000 cal · 1 cal = 4.184 J · 1 kJ = 1000 J
given: 230 Cal · wanted: kJ

A common first attempt

230 cal × 4.184 J1 cal × 1 kJ1000 J = 0.962 kJ ✗
Dr. Karmach

Worked example 3: solution

1 Cal = 1000 cal · 1 cal = 4.184 J · 1 kJ = 1000 J
given: 230 Cal · wanted: kJ

A common first attempt

230 cal × 4.184 J1 cal × 1 kJ1000 J = 0.962 kJ ✗
The kilojoule label reads 960: this result is 1000 times too small. The label's unit is Cal, not cal. ✗
Dr. Karmach

Worked example 3: the correct chain

1 Cal = 1000 cal · 1 cal = 4.184 J · 1 kJ = 1000 J
given: 230 Cal · wanted: kJ

Step 2 · Plan the route

The capital C marks the food Calorie: 1 Cal = 1000 cal. The route: Cal → cal → J → kJ. Three conversion factors are needed.

Dr. Karmach

Worked example 3: the correct chain

1 Cal = 1000 cal · 1 cal = 4.184 J · 1 kJ = 1000 J
given: 230 Cal · wanted: kJ
Step 2 · Plan the route Step 3 · Chain the factors so each unit cancels
230 Cal × 1000 cal1 Cal × 4.184 J1 cal × 1 kJ1000 J = 962 kJ
Dr. Karmach

Worked example 3: the correct chain

1 Cal = 1000 cal · 1 cal = 4.184 J · 1 kJ = 1000 J
given: 230 Cal · wanted: kJ
Step 2 · Plan the route Step 3 · Chain the factors so each unit cancels
230 Cal × 1000 cal1 Cal × 4.184 J1 cal × 1 kJ1000 J = 962 kJ
Step 4 · Sense-check
The kilojoule label reads 960: the chain reproduces it, rounded. The same chain shows 1 Cal = 4.184 kJ. ✓
Dr. Karmach

Worked example 3: the route on the map

1 Cal = 1000 cal · 1 cal = 4.184 J · 1 kJ = 1000 J
given: 230 Cal · found: 962 kJ

Three edges, three conversion factors. The trip around the map reproduces the top edge: 1 Cal = 4.184 kJ. ✓
Dr. Karmach

Take-home: the food Calorie is a kilocalorie

Do: read the capital C as 1000 cal. Big C, big unit.

230 Cal × (1000 cal / 1 Cal) × (4.184 J / 1 cal) × (1 kJ / 1000 J) = 962 kJ
matches the 960 kJ label ✓

Do not: read Cal as cal. The answer lands 1000 times too small.

230 cal × (4.184 J / 1 cal) × (1 kJ / 1000 J) = 0.962 kJ
1000 times smaller than the label ✗
Dr. Karmach

Practice 3

1 Cal = 1000 cal · 1 cal = 4.184 J · 1 kJ = 1000 J
given: 205 Cal · wanted: cal, J and kJ

One cup of cooked rice provides 205 Calories. How much energy is that in calories, in joules and in kilojoules?

  1. cal: 205 · J: 858 · kJ: 0.858
  2. cal: 2.05 × 10⁵ · J: 8.58 × 10⁵ · kJ: 858
  3. cal: 2.05 × 10⁵ · J: 4.90 × 10⁴ · kJ: 49.0
  4. cal: 2.05 × 10⁵ · J: 858 · kJ: 858
  5. cal: 2.05 × 10⁵ · J: 8.58 × 10⁵ · kJ: 8.58 × 10⁸
Dr. Karmach

Practice 3 · answer: B

205 Cal = 2.05 × 10⁵ cal = 8.58 × 10⁵ J = 858 kJ (answer B)
given: 205 Cal · 1 Cal = 1000 cal · 1 cal = 4.184 J · 1 kJ = 1000 J · each hop reported
205 Cal × 1000 cal1 Cal × 4.184 J1 cal × 1 kJ1000 J = 858 kJ

A read Cal as cal: each value a thousand times too small. C flipped 4.184: 2.05 × 10⁵ / 4.184 = 4.90 × 10⁴ J. D wrote the kJ number as the J count: 858 kJ = 8.58 × 10⁵ J. E multiplied by 1000 at the last hop.

After the chain, check with 1 Cal = 4.184 kJ: 205 × 4.184 = 858. ✓
Dr. Karmach

Practice 4

1 Cal = 1000 cal · 1 cal = 4.184 J · 1 kJ = 1000 J
given: 8.50 Cal per minute · 40.0 min · wanted: kJ

Swimming laps burns about 8.50 Calories per minute. How many kilojoules do 40.0 minutes of laps use?

  1. 1.42
  2. 81.3
  3. 340.
  4. 1.42 × 10³
Dr. Karmach

Practice 4 · answer: D

1 Cal = 1000 cal · 1 cal = 4.184 J · 1 kJ = 1000 J
given: 8.50 Cal per minute · 40.0 min · plan: min → Cal → cal → J → kJ
40.0 min × 8.50 Cal1 min = 340. Cal
340. Cal × 1000 cal1 Cal × 4.184 J1 cal × 1 kJ1000 J = 1.42 × 10³ kJ (answer D)

A read Cal as cal: 340. × 4.184 / 1000 = 1.42, a thousand times too small. B flipped the 4.184 factor: 340. × 1000 / 4.184 / 1000 = 81.3, and the joule never cancels. C stopped at Calories: 340. is the energy in Cal, never converted to kJ.

One food Calorie is 4.184 kJ, so 340 Cal sits near 340 × 4 = 1360 kJ. The chain gives 1.42 × 10³. ✓
Dr. Karmach

Check yourself

  1. A label lists 95 Calories. Write the chain to kilojoules: which factor comes first, and what does each unit cancel into?
  2. A cup of water and a pot of water both read 60 °C. Which quantity matches, and which differs: temperature, or energy content?

Every joule a system gains or loses arrives as heat (q) or as work (w). The first law adds them: ΔE = q + w. At constant pressure the heat term earns its own name, the enthalpy change ΔH.

Dr. Karmach

2 · Exothermic & Endothermic

Classify any process as exothermic or endothermic (from the sign of ΔH, from an energy diagram, or from a heat term written into the equation) and state which way heat flows between system and surroundings.

Dr. Karmach

Two pouches from the drugstore

Snap the pouch inside a hand warmer and it climbs to 54 °C. Snap a cold pack and it drops near freezing. Sealed chemicals drive both changes.

Dr. Karmach

The system and its surroundings

The reaction is the system; the flask, your hand, the room are the surroundings. ΔH records the system's heat: out negative, in positive. The sign follows the system, not your hand.

Dr. Karmach

Enthalpy

Enthalpy, H, is the heat content of a system. A change in it, ΔH, equals the heat of the process at constant pressure. An open flask or a pouch in your hand qualifies.

ΔH = heat of the process at constant pressure
heat out of the system → ΔH negative · heat in → ΔH positive
Dr. Karmach

Exothermic and endothermic

exothermic: heat exits the system
surroundings warm up · ΔH negative · burning fuel, the hand-warmer pouch
endothermic: heat enters the system
surroundings cool down · ΔH positive · melting ice, the cold-pack pouch
memory hook: EXo, heat EXits · ENdo, heat ENters
the prefix names the heat's direction, read from the system's side

Heat "flows from a hot object to a cold object". A process sending heat out is exothermic; one taking heat in is endothermic. Both names describe the system; the surroundings show the opposite change.

Dr. Karmach

Energy diagrams

An energy diagram plots energy against reaction progress. Products below the reactants: the difference left as heat, exothermic. Products above: the difference came in as heat, endothermic.

Dr. Karmach

Heat written into the equation

CH₄(g) + 2 O₂(g) → CO₂(g) + 2 H₂O(l) + 890 kJ
heat on the product side: it leaves with the products · ΔH = −890 kJ · exothermic
2 H₂O(l) + 572 kJ → 2 H₂(g) + O₂(g)
heat on the reactant side: it must be supplied · ΔH = +572 kJ · endothermic

A thermochemical equation may carry its heat in-line. Product side: heat released, exothermic. Reactant side: heat absorbed, endothermic. The separate ΔH states the same fact with a sign.

Dr. Karmach

The method

  1. Name the system. The process is the system; all else is surroundings.
  2. Find the heat's direction. From the ΔH sign, diagram levels, or heat term.
  3. State the verdict. Heat out: exothermic, ΔH negative. Heat in: endothermic, ΔH positive.
Dr. Karmach

Worked example 1: a hand warmer's reaction

4 Fe(s) + 3 O₂(g) → 2 Fe₂O₃(s) · ΔH = −1648 kJ
given: the equation and its ΔH · wanted: the verdict and the heat's direction

Inside a hand warmer, iron powder reacts with oxygen from the air.

Classify the reaction and state which way heat flows.

Dr. Karmach

Worked example 1: solution

4 Fe(s) + 3 O₂(g) → 2 Fe₂O₃(s) · ΔH = −1648 kJ
given: the equation and its ΔH

Step 1 · Name the system

The iron and oxygen are the system. The pouch, the air, your cold hands: surroundings.

Dr. Karmach

Worked example 1: solution

4 Fe(s) + 3 O₂(g) → 2 Fe₂O₃(s) · ΔH = −1648 kJ
given: the equation and its ΔH
Step 1 · Name the system Step 2 · Find the heat's direction

ΔH is negative: −1648 kJ. Negative marks heat leaving the system.

Dr. Karmach

Worked example 1: solution

4 Fe(s) + 3 O₂(g) → 2 Fe₂O₃(s) · ΔH = −1648 kJ
given: the equation and its ΔH
Step 1 · Name the system Step 2 · Find the heat's direction Step 3 · State the verdict
4 Fe(s) + 3 O₂(g) → 2 Fe₂O₃(s) + 1648 kJ → exothermic
heat out · ΔH = −1648 kJ · the surroundings (your hands) warm up
Dr. Karmach

Worked example 1: solution

4 Fe(s) + 3 O₂(g) → 2 Fe₂O₃(s) · ΔH = −1648 kJ
given: the equation and its ΔH
Step 1 · Name the system Step 2 · Find the heat's direction Step 3 · State the verdict
4 Fe(s) + 3 O₂(g) → 2 Fe₂O₃(s) + 1648 kJ → exothermic
heat out · ΔH = −1648 kJ · the surroundings (your hands) warm up
The pouch warms your hand: the surroundings gain exactly the heat the system loses. A negative ΔH and a warming hand agree.
Dr. Karmach

Worked example 1: the clue used

4 Fe(s) + 3 O₂(g) → 2 Fe₂O₃(s) · ΔH = −1648 kJ
clue read: the sign of ΔH · verdict: exothermic

Any one of the three clues gives the heat's direction. Here the sign settled it: negative, heat out, exothermic. ✓
Dr. Karmach

Worked example 2: hydrogen peroxide decomposes

2 H₂O₂(l) → 2 H₂O(l) + O₂(g)
given: the energy diagram · wanted: the verdict and ΔH with its sign

Hydrogen peroxide fizzing on a cut breaks down into water and oxygen. Classify the process from the diagram and give ΔH.

Dr. Karmach

Worked example 2: solution

Step 1 · Name the system

The decomposing peroxide is the system; the cut, the skin, the air are surroundings.

Dr. Karmach

Worked example 2: solution


Step 1 · Name the system
Step 2 · Find the heat's direction

The products sit 196 kJ below the reactants. That difference left the system as heat.

Dr. Karmach

Worked example 2: solution


Step 1 · Name the system
Step 2 · Find the heat's direction
Step 3 · State the verdict

2 H₂O₂(l) → 2 H₂O(l) + O₂(g) → exothermic
products lower · heat out · ΔH = −196 kJ
Dr. Karmach

Worked example 2: solution


Step 1 · Name the system
Step 2 · Find the heat's direction
Step 3 · State the verdict

2 H₂O₂(l) → 2 H₂O(l) + O₂(g) → exothermic
products lower · heat out · ΔH = −196 kJ
Downhill on an energy diagram is heat out. The products hold less energy than the reactants, and the fizzing cut warms slightly.
Dr. Karmach

Worked example 2: the clue used

2 H₂O₂(l) → 2 H₂O(l) + O₂(g)
clue read: the energy-diagram levels · verdict: exothermic, ΔH = −196 kJ

No ΔH was written, and none was needed for the direction: products below the reactants is heat out. ✓
Dr. Karmach

Your turn: photosynthesis

6 CO₂(g) + 6 H₂O(l) + 2803 kJ → C₆H₁₂O₆(s) + 6 O₂(g)
a leaf builds glucose; the 2803 kJ arrives as sunlight
step question answer
1 · name the system what is changing? the CO₂ and water becoming glucose
2 · find the heat's direction which side carries the heat term? the side; heat the system
3 · state the verdict · ΔH = kJ

Complete the three steps.

Dr. Karmach

Your turn: photosynthesis

6 CO₂(g) + 6 H₂O(l) + 2803 kJ → C₆H₁₂O₆(s) + 6 O₂(g)
a leaf builds glucose; the 2803 kJ arrives as sunlight
step question answer
1 · name the system what is changing? the CO₂ and water becoming glucose
2 · find the heat's direction which side carries the heat term? the side; heat the system
3 · state the verdict · ΔH = kJ

Complete the three steps.

photosynthesis → endothermic
heat term on the reactant side · heat enters the system · ΔH = +2803 kJ
Dr. Karmach

Your turn: the clue used

6 CO₂(g) + 6 H₂O(l) + 2803 kJ → C₆H₁₂O₆(s) + 6 O₂(g)
clue read: the side of the heat term · verdict: endothermic, ΔH = +2803 kJ

A heat term with the reactants is heat the system must take in. Reactant side, heat in, endothermic. ✓
Dr. Karmach

Where this goes wrong

Reading the sign from your hand. A cold pack chills your skin, and the chill gets recorded as heat lost: ΔH = −26 kJ. The skin is surroundings. Its loss is the system's gain: ΔH = +26 kJ.
Pairing a label with the opposite flow. "Exothermic, and it absorbs heat" contradicts itself. The label names the flow: exothermic releases heat, endothermic absorbs it. One verdict carries both parts.
Reading the heat term from the wrong side. In 2 H₂O(l) + 572 kJ → 2 H₂(g) + O₂(g), the 572 kJ gets reported as released. It sits with the reactants, so it is consumed: absorbed, ΔH = +572 kJ.
Calling the higher level the bigger release. Height on an energy diagram is energy stored, not energy given off. Products above the reactants means the system took energy in: endothermic, ΔH positive.
Dr. Karmach

Practice 1

2 SO₂(g) + O₂(g) → 2 SO₃(g) · ΔH = −198 kJ
given: the equation and its ΔH

Sulfur dioxide converts to sulfur trioxide during sulfuric acid manufacture. Which statement describes the reaction?

  1. Endothermic: heat is absorbed by the system from the surroundings
  2. Exothermic: heat is absorbed by the system from the surroundings
  3. Exothermic: heat is released by the system to the surroundings
  4. Endothermic: heat is released by the system to the surroundings
Dr. Karmach

Practice 1 · answer: C

ΔH = −198 kJ → negative → heat out → exothermic (answer C)
heat released by the system · the surroundings warm up

A flipped the sign convention: heat absorbed would be counted into the system, +198 kJ, not −198 kJ. B paired the right label with the wrong flow: exothermic means heat exits the system. D paired the right flow with the wrong label: a heat-releasing reaction is exothermic.

Negative ΔH, heat out, exothermic, warmer surroundings: four readings of the same event.
Dr. Karmach

Worked example 3: the cold pack

NH₄NO₃(s) → NH₄NO₃(aq)
given: the pouch turns icy in your hand · wanted: the verdict and the sign of ΔH

Snapping the pack lets ammonium nitrate dissolve in water, and the pouch turns icy.

A common first answer: the pack is cold, so it is losing heat: exothermic. Test it.

Dr. Karmach

Worked example 3: solution

NH₄NO₃(s) → NH₄NO₃(aq)
the pouch turns icy in your hand

A common first answer

cold pack, so the pack is losing heat → exothermic?
cold marks heat leaving the pack only if the pack were the surroundings ✗

The cold skin is the evidence. Your hand is losing heat, and the hand is surroundings, not system.

Dr. Karmach

Worked example 3: solution

NH₄NO₃(s) → NH₄NO₃(aq)
the pouch turns icy in your hand
A common first answer
cold pack, so the pack is losing heat → exothermic?
cold marks heat leaving the pack only if the pack were the surroundings ✗
Step 1 · Name the system

The dissolving salt and water are the system. The pouch, your hand: surroundings.

Dr. Karmach

Worked example 3: solution

NH₄NO₃(s) → NH₄NO₃(aq)
the pouch turns icy in your hand
A common first answer
cold pack, so the pack is losing heat → exothermic?
cold marks heat leaving the pack only if the pack were the surroundings ✗
Step 1 · Name the system Step 2 · Find the heat's direction

Your hand cools: heat is leaving the surroundings and entering the system.

Dr. Karmach

Worked example 3: solution

NH₄NO₃(s) → NH₄NO₃(aq)
the pouch turns icy in your hand
A common first answer
cold pack, so the pack is losing heat → exothermic?
cold marks heat leaving the pack only if the pack were the surroundings ✗
Step 1 · Name the system Step 2 · Find the heat's direction Step 3 · State the verdict
NH₄NO₃(s) → NH₄NO₃(aq) → endothermic
heat in · measured ΔH = +26 kJ per mole dissolved · the surroundings (your hand) cool
Dr. Karmach

Worked example 3: solution

NH₄NO₃(s) → NH₄NO₃(aq)
the pouch turns icy in your hand
A common first answer
cold pack, so the pack is losing heat → exothermic?
cold marks heat leaving the pack only if the pack were the surroundings ✗
Step 1 · Name the system Step 2 · Find the heat's direction Step 3 · State the verdict
NH₄NO₃(s) → NH₄NO₃(aq) → endothermic
heat in · measured ΔH = +26 kJ per mole dissolved · the surroundings (your hand) cool
The pack feels cold *because* it absorbs heat. A cooling hand is the surroundings' loss and the system's gain: ΔH = +26 kJ, never −26 kJ.
Dr. Karmach

Take-home: your hand is the surroundings

feels hot → the surroundings are gaining heat → the system is losing it
exothermic · ΔH negative
feels cold → the surroundings are losing heat → the system is gaining it
endothermic · ΔH positive

Skin and thermometers sit in the surroundings. They report the surroundings' change, and the system did the opposite. Feels cold: the system is absorbing heat: endothermic, ΔH positive.

Dr. Karmach

Practice 2: everyday changes

process
1 water evaporates from a puddle
2 snow forms in a cloud
3 a strong acid is mixed with a strong base

Classify each process, in order, as exothermic or endothermic.

  1. endothermic · endothermic · exothermic
  2. endothermic · exothermic · exothermic
  3. exothermic · exothermic · exothermic
  4. endothermic · exothermic · endothermic
Dr. Karmach

Practice 2: answer B

endothermic · exothermic · exothermic (answer B)
evaporating: heat in · water turning to ice: heat out · acid and base mixed: heat out

A took every change of state as heat in. Melting takes heat in, so its reverse, water turning to ice, gives heat out. C read evaporation's cooling as heat out. The cooling is the surroundings giving the evaporating water its heat. D assumed a reaction must absorb energy to happen; the acid and base mixture turns warm.

Evaporation cools the ground it leaves; an acid and base mixture warms its beaker. Each is the surroundings reporting, and the system does the opposite. ✓
Dr. Karmach

Practice 3: water gas

C(s) + H₂O(g) → CO(g) + H₂(g)
given: the energy diagram

Steam over red-hot coke makes water gas, a fuel. Which statement describes the reaction?

  1. Exothermic, ΔH = −131 kJ
  2. Endothermic, ΔH = −131 kJ
  3. Exothermic, ΔH = +131 kJ
  4. Endothermic, ΔH = +131 kJ
Dr. Karmach

Practice 3: answer D

C(s) + H₂O(g) → CO(g) + H₂(g) → endothermic, ΔH = +131 kJ (answer D)
products 131 kJ above the reactants · the system took that energy in

A called the higher level the bigger release: height is energy stored, so products above the reactants took energy in. B took the sign from the surroundings: the furnace loses 131 kJ, and the system gains it, +131 kJ. C paired the positive sign with the wrong label: heat in is endothermic.

Uphill on an energy diagram is heat in. The coke must be kept red-hot for the reaction to run: endothermic, ΔH positive. ✓
Dr. Karmach

Practice 4

CaO(s) + H₂O(l) → Ca(OH)₂(s) + 65 kJ
given: the equation · the bucket turns hot

Water is stirred into quicklime and the bucket turns hot. A classmate writes: "The 65 kJ ends up with the products, so the system gains heat: endothermic, ΔH = +65 kJ." What is wrong with the reasoning, if anything?

  1. Heat written with the products is released: exothermic, ΔH = −65 kJ. The hot bucket is the surroundings.
  2. Nothing is wrong: heat written with the products is heat gained, so ΔH = +65 kJ.
  3. Only the label is wrong: ΔH = +65 kJ stands, but a hot bucket means exothermic.
  4. Only the sign is wrong: it is endothermic, but heat that warms the bucket is −65 kJ.
Dr. Karmach

Practice 4 · answer: A

CaO(s) + H₂O(l) → Ca(OH)₂(s) + 65 kJ → exothermic, ΔH = −65 kJ (answer A)
heat term on the product side: released · the hot bucket is the surroundings gaining that heat

B read a product-side heat term as heat gained: it leaves with the products, so it is released, −65 kJ, not +65 kJ. C matched the sign but not the label: a positive ΔH would mean heat in, and a bucket cannot turn hot from that. D matched the label but not the sign: endothermic and ΔH = −65 kJ contradict each other.

Two pieces of evidence, one verdict: the heat term sits with the products, and the surroundings warm. Heat out, exothermic, ΔH negative.
Dr. Karmach

Extra practice 1

Ba(OH)₂·8H₂O(s) + 2 NH₄Cl(s) → BaCl₂(aq) + 2 NH₃(aq) + 10 H₂O(l)
given: the flask rests on a wet wooden board · the water under it freezes

Two white solids are stirred together in a flask on a wet board, and within minutes the water under the flask freezes. Which statement describes the reaction?

  1. Exothermic, ΔH negative: heat flows from the flask into the board
  2. Exothermic, ΔH positive: heat flows from the board into the flask
  3. Endothermic, ΔH positive: heat flows from the board into the flask
  4. Endothermic, ΔH negative: heat flows from the board into the flask
Dr. Karmach

Extra practice 1 · answer: C

Ba(OH)₂·8H₂O(s) + 2 NH₄Cl(s) → BaCl₂(aq) + 2 NH₃(aq) + 10 H₂O(l)
surroundings: the board and its water · heat flows board → flask · endothermic, ΔH positive (answer C)

A took the freezing as the reaction's own change. Freezing does release heat, but the water is surroundings, and its heat went into the flask. B paired the label with the wrong flow: heat into the system is endothermic. D read the sign from the surroundings: the board loses heat, the system gains it, so ΔH is positive.

Water freezes only when heat is pulled out of it. The flask pulled it out: the system absorbed heat, endothermic, ΔH positive. ✓
Dr. Karmach

Extra practice 2

2 HgO(s) + 43.4 kcal → 2 Hg(l) + O₂(g)
given: the heat term in kcal · 1 cal = 4.184 J

Strong heating breaks red mercury(II) oxide into mercury and oxygen. What is ΔH for the reaction, in kJ, sign included?

  1. +182
  2. −182
  3. +10.4
  4. +0.182
  5. +43.4
Dr. Karmach

Extra practice 2 · answer: A

2 HgO(s) + 43.4 kcal → 2 Hg(l) + O₂(g) → endothermic
heat term on the reactant side: absorbed · ΔH positive

Three conversion factors are needed: kcal → cal → J → kJ.

43.4 kcal × 1000 cal1 kcal × 4.184 J1 cal × 1 kJ1000 J = +182 kJ · answer A

B read the heat term from the wrong side: it sits with the reactants, so it is absorbed, +182 kJ. C flipped the 4.184 factor: 43.4 ÷ 4.184 = 10.4. D read kcal as cal: 43.4 × 4.184 = 182 J, only 0.182 kJ. E skipped the conversion: 43.4 is the heat in kcal, not kJ.

A kilojoule is smaller than a kilocalorie, so the kJ value must be the larger number: 43.4 × 4.184 = 182. ✓
Dr. Karmach

Check yourself

  1. Propane burns in a camp stove: C₃H₈(g) + 5 O₂(g) → 3 CO₂(g) + 4 H₂O(l), ΔH = −2220 kJ. State the verdict and which way heat flows.
  2. An energy diagram shows the products 178 kJ above the reactants. Give the sign of ΔH and the verdict.

Exothermic or endothermic names the heat's direction. How much heat a sample gains or loses depends on its mass, its substance, and its temperature change: q = m·c·ΔT.

Dr. Karmach

3 · Specific Heat & q = mcΔT

Use q = m·c·ΔT to find the heat, the mass, the specific heat, or the temperature change, with ΔT measured final minus initial so the sign of q shows which way the heat flowed.

Dr. Karmach

One burner, two temperatures

Five minutes in, the iron handle is too hot to touch; the water is barely warm. Iron needs far less heat than water for each degree it climbs.

Dr. Karmach

Specific heat: joules per gram per degree

specific heat c: the heat that raises 1 g of a substance by 1 °C
J/g·°C: water 4.184 · ethyl alcohol 2.46 · aluminum 0.897 · iron 0.449 · copper 0.385 · gold 0.129 · lead 0.128

Heat flowing in raises a substance's temperature; heat flowing out lowers it. The joules needed to move each gram by one degree are fixed for each substance: its specific heat, c.

Dr. Karmach

The heat equation

Three factors set the heat: the mass m, the substance's specific heat c, and the temperature change ΔT. One equation, four solvable quantities.

Dr. Karmach

ΔT carries a sign

ΔT = Tfinal − Tinitial
heating 20.0 → 50.0 °C: ΔT = +30.0 °C · cooling 50.0 → 20.0 °C: ΔT = −30.0 °C

ΔT is final minus initial, in that order. A cooling sample has a negative ΔT, so q comes out negative: the sample released heat. The sign records the direction of the flow.

Dr. Karmach

Specific heat c vs heat capacity C

C = m · c
60.0 g of water: C = 60.0 g × 4.184 J/g·°C = 251 J/°C · c stays 4.184 J/g·°C for any amount of water

Specific heat is intensive: per gram, the same for a drop or a lake. Heat capacity C is extensive: it grows with the sample, because m is in it.

memory hook: little c, one gram · big C, the whole sample
the food Calorie's cue again: the capital letter marks the bigger quantity
Dr. Karmach

The method

  1. List the pieces: m, c, ΔT = Tfinal − Tinitial. Mark the unknown.
  2. Rearrange for the unknown before numbers go in.
  3. Substitute and cancel units.
  4. Check the sign: cooling means negative ΔT and negative q.
Dr. Karmach

Worked example 1: heat to warm water

q = m · c · ΔT
given: 250 g water · c = 4.184 J/g·°C · 20.0 °C → 50.0 °C · wanted: q

A kettle warms 250 g of water from 20.0 °C to 50.0 °C. How much heat does the water absorb? (c of water: 4.184 J/g·°C)

List the pieces: m, c, and ΔT = Tfinal − Tinitial.

Dr. Karmach

Worked example 1: solution

q = m · c · ΔT
given: 250 g water · c = 4.184 J/g·°C · 20.0 °C → 50.0 °C · wanted: q

Step 1 · List the pieces

m = 250 g. c = 4.184 J/g·°C. ΔT = 50.0 − 20.0 = +30.0 °C. The unknown is q.

Dr. Karmach

Worked example 1: solution

q = m · c · ΔT
given: 250 g water · c = 4.184 J/g·°C · 20.0 °C → 50.0 °C · wanted: q
Step 1 · List the pieces Step 2 · Rearrange for the unknown

q already stands alone on its side of the equation; no rearranging is needed.

Dr. Karmach

Worked example 1: solution

q = m · c · ΔT
given: 250 g water · c = 4.184 J/g·°C · 20.0 °C → 50.0 °C · wanted: q
Step 1 · List the pieces Step 2 · Rearrange for the unknown Step 3 · Substitute and cancel units
q = 250 g × 4.184 J1 g·°C × 30.0 °C = 31,400 J
Dr. Karmach

Worked example 1: solution

q = m · c · ΔT
given: 250 g water · c = 4.184 J/g·°C · 20.0 °C → 50.0 °C · wanted: q
Step 1 · List the pieces Step 2 · Rearrange for the unknown Step 3 · Substitute and cancel units
q = 250 g × 4.184 J1 g·°C × 30.0 °C = 31,400 J
Step 4 · Check the sign
The water warmed, so ΔT and q are both positive: 31,400 J (31.4 kJ) absorbed. More grams or more degrees would cost more heat. ✓
Dr. Karmach

Worked example 1: solving for q

q = m · c · ΔT
given: 250 g water · c = 4.184 J/g·°C · ΔT = +30.0 °C · found: q = 31,400 J

q is the unknown, so no rearranging: m, c and ΔT go straight in. ✓
Dr. Karmach

Worked example 2: find c, identify the substance

q = m · c · ΔT
given: q = 1347 J · m = 125 g · 22.0 °C → 46.0 °C · wanted: c

A 125-g metal block absorbs 1347 J as it warms from 22.0 °C to 46.0 °C. Candidate specific heats, in J/g·°C:

aluminum iron copper gold lead
0.897 0.449 0.385 0.129 0.128

Find the block's specific heat and match it to the table.

Dr. Karmach

Worked example 2: solution

q = m · c · ΔT
given: q = 1347 J · m = 125 g · 22.0 °C → 46.0 °C · wanted: c

Step 1 · List the pieces

q = 1347 J. m = 125 g. ΔT = 46.0 − 22.0 = +24.0 °C. The unknown is c.

Dr. Karmach

Worked example 2: solution

q = m · c · ΔT
given: q = 1347 J · m = 125 g · 22.0 °C → 46.0 °C · wanted: c
Step 1 · List the pieces Step 2 · Rearrange for the unknown
q = m · c · ΔT → c = qm · ΔT

Divide both sides by m·ΔT before any numbers go in.

Dr. Karmach

Worked example 2: solution

q = m · c · ΔT
given: q = 1347 J · m = 125 g · 22.0 °C → 46.0 °C · wanted: c
Step 1 · List the pieces Step 2 · Rearrange for the unknown
q = m · c · ΔT → c = qm · ΔT
Step 3 · Substitute and cancel units
c = 1347 J125 g × 24.0 °C = 0.449 J/g·°C

No unit cancels here; they assemble into J/g·°C: the unit of a specific heat.

Dr. Karmach

Worked example 2: solution

q = m · c · ΔT
given: q = 1347 J · m = 125 g · 22.0 °C → 46.0 °C · wanted: c
Step 1 · List the pieces Step 2 · Rearrange for the unknown
q = m · c · ΔT → c = qm · ΔT
Step 3 · Substitute and cancel units
c = 1347 J125 g × 24.0 °C = 0.449 J/g·°C
0.449 J/g·°C sits in the range of a metal's specific heat, ready to identify. ✓
Dr. Karmach

Worked example 2: identify the metal

c = 0.449 J/g·°C
from q = 1347 J · m = 125 g · ΔT = +24.0 °C, both positive

Match the property

aluminum iron copper gold lead
0.897 0.449 0.385 0.129 0.128

Only iron matches 0.449 J/g·°C. The block is iron.

Dr. Karmach

Worked example 2: identify the metal

c = 0.449 J/g·°C
from q = 1347 J · m = 125 g · ΔT = +24.0 °C, both positive
Match the property
aluminum iron copper gold lead
0.897 0.449 0.385 0.129 0.128

Step 4 · Check the sign

The block warmed: ΔT and q are both positive. Plug back in: 125 g × 0.449 J/g·°C × 24.0 °C returns 1347 J. ✓
Dr. Karmach

Worked example 2: solving for c

q = m · c · ΔT
given: q = 1347 J · m = 125 g · ΔT = +24.0 °C · found: c = 0.449 J/g·°C, iron

c is the unknown. Dividing both sides by m · ΔT isolates it before any numbers go in. ✓
Dr. Karmach

Your turn: mass of ethyl alcohol

q = m · c · ΔT
given: q = 8020 J · c = 2.46 J/g·°C · 18.0 °C → 43.0 °C · wanted: m

Ethyl alcohol (c = 2.46 J/g·°C) absorbs 8020 J and warms from 18.0 °C to 43.0 °C.

m = qc · ΔT = 8020 J J/g·°C × °C = g

Fill in c and ΔT = Tfinal − Tinitial, then compute the mass.

Dr. Karmach

Your turn: mass of ethyl alcohol

q = m · c · ΔT
given: q = 8020 J · c = 2.46 J/g·°C · 18.0 °C → 43.0 °C · wanted: m

Ethyl alcohol (c = 2.46 J/g·°C) absorbs 8020 J and warms from 18.0 °C to 43.0 °C.

m = qc · ΔT = 8020 J J/g·°C × °C = g

Fill in c and ΔT = Tfinal − Tinitial, then compute the mass.

m = 8020 J2.46 J/g·°C × 25.0 °C = 130. g
2.46 J warms one gram by one degree, so 8020 J spread over 25.0 degrees warms about 130 g. ✓
Dr. Karmach

Where this goes wrong

q = m · c · ΔT
250 g water · c = 4.184 J/g·°C · 20.0 → 50.0 °C · correct q = 31,400 J
Leaving out the mass. 4.184 × 30.0 = 126 J is the heat for a single gram. The sample has 250 of them. All three factors multiply: q = m·c·ΔT = 31,400 J.
Leaving out the temperature change. 250 × 4.184 = 1046 J warms the water by one degree only. Multiply by the full ΔT of 30.0 °C.
Dividing by the specific heat. 250 × 30.0 ÷ 4.184 = 1790, and its units are g²·°C²/J, not joules. c multiplies on top: (4.184 J / 1 g·°C).
Subtracting the temperatures in the wrong order. ΔT = 20.0 − 50.0 = −30.0 °C gives q = −31,400 J: heat released by water that is warming. ΔT is Tfinal − Tinitial.
Dr. Karmach

Practice 1

q = m · c · ΔT
given: 75.0 g copper · c = 0.385 J/g·°C · ΔT = +20.0 °C · wanted: q

A 75.0-g copper fitting warms by 20.0 °C as hot water flows past it. How much heat, in J, does the copper absorb? (c of copper: 0.385 J/g·°C)

  1. 7.70
  2. 28.9
  3. 578
  4. 3.90 × 10³
Dr. Karmach

Practice 1 · answer: C

q = m · c · ΔT
given: 75.0 g copper · c = 0.385 J/g·°C · ΔT = +20.0 °C
q = 75.0 g × 0.385 J1 g·°C × 20.0 °C = 578 J (answer C)

A left out the mass: 0.385 × 20.0 = 7.70 J warms one gram. B left out the temperature change: 75.0 × 0.385 = 28.9 J is one degree's worth. D divided by the specific heat: 75.0 × 20.0 ÷ 0.385 = 3.90 × 10³, with units g²·°C²/J.

Copper takes only 0.385 J per gram per degree, but 75 grams and 20 degrees multiply that into hundreds of joules. ✓
Dr. Karmach

Worked example 3: final temperature of a cooling sample

q = m · c · ΔT
given: 150 g aluminum · c = 0.897 J/g·°C · Tinitial = 95.0 °C · releases 8100 J · wanted: Tfinal

A 150-g aluminum pan lid at 95.0 °C releases 8100 J as it cools. What is its final temperature? (c of aluminum: 0.897 J/g·°C)

A common first attempt: substitute 8100 J with no sign. Test the result.

Dr. Karmach

Worked example 3: solution

q = m · c · ΔT
given: 150 g aluminum · c = 0.897 J/g·°C · Tinitial = 95.0 °C · releases 8100 J · wanted: Tfinal

A common first attempt

ΔT = +8100 J150 g × 0.897 J/g·°C = +60.2 °C → Tfinal = 95.0 + 60.2 = 155.2 °C ✗

A lid that is releasing heat cannot end up hotter. The sign of q was dropped.

Dr. Karmach

Worked example 3: solution

q = m · c · ΔT
given: 150 g aluminum · c = 0.897 J/g·°C · Tinitial = 95.0 °C · releases 8100 J · wanted: Tfinal
A common first attempt
ΔT = +8100 J150 g × 0.897 J/g·°C = +60.2 °C → Tfinal = 95.0 + 60.2 = 155.2 °C ✗
Step 1 · List the pieces

Released heat leaves the sample, so q = −8100 J. m = 150 g. c = 0.897 J/g·°C. The unknown is ΔT, then Tfinal.

Dr. Karmach

Worked example 3: solution

q = m · c · ΔT
given: 150 g aluminum · c = 0.897 J/g·°C · Tinitial = 95.0 °C · releases 8100 J · wanted: Tfinal
A common first attempt
ΔT = +8100 J150 g × 0.897 J/g·°C = +60.2 °C → Tfinal = 95.0 + 60.2 = 155.2 °C ✗
Step 1 · List the pieces Step 2 · Rearrange for the unknown
ΔT = qm · c , then Tfinal = Tinitial + ΔT
With q entered as −8100 J, the formula is set to return a negative ΔT: a temperature drop. ✓
Dr. Karmach

Worked example 3: final temperature

q = −8100 J released · 150 g aluminum · c = 0.897 J/g·°C
Tinitial = 95.0 °C · wanted: Tfinal

Step 3 · Substitute and cancel units

ΔT = −8100 J150 g × 0.897 J/g·°C = −8100 J134.55 J/°C = −60.2 °C
Tfinal = 95.0 °C + (−60.2 °C) = 34.8 °C
Dr. Karmach

Worked example 3: final temperature

q = −8100 J released · 150 g aluminum · c = 0.897 J/g·°C
Tinitial = 95.0 °C · wanted: Tfinal
Step 3 · Substitute and cancel units
ΔT = −8100 J150 g × 0.897 J/g·°C = −8100 J134.55 J/°C = −60.2 °C
Tfinal = 95.0 °C + (−60.2 °C) = 34.8 °C
Step 4 · Check the sign
Released heat means negative q, negative ΔT, and a lower final temperature: 95.0 → 34.8 °C. ✓ The signless route predicted 155.2 °C, a cooling lid ending hotter. ✗
Dr. Karmach

Worked example 3: solving for ΔT, then Tfinal

q = −8100 J · 150 g aluminum · c = 0.897 J/g·°C · Tinitial = 95.0 °C
found: ΔT = −60.2 °C · Tfinal = 34.8 °C

ΔT is a change, not an end point. Tfinal = 95.0 + (−60.2) = 34.8 °C. ✓
Dr. Karmach

Take-home: ΔT is final minus initial

warming: 20.0 °C → 50.0 °C · ΔT = 50.0 − 20.0 = +30.0 °C · q positive
heat absorbed ✓
cooling: 95.0 °C → 34.8 °C · ΔT = 34.8 − 95.0 = −60.2 °C · q negative
heat released ✓

ΔT is always Tfinal − Tinitial, and released heat enters as negative q. The sign is part of the quantity; it records which way the heat flowed.

Dr. Karmach

Practice 2

q = m · c · ΔT
given: 100. g lead · c = 0.128 J/g·°C · 62.0 °C → 22.0 °C · wanted: q

A 100.-g lead sinker at 62.0 °C drops into a stream and cools to 22.0 °C. What is q for the lead, in J? (c of lead: 0.128 J/g·°C)

  1. 512
  2. −512
  3. 12.8
  4. −5.12
Dr. Karmach

Practice 2 · answer: B

q = m · c · ΔT
given: 100. g lead · c = 0.128 J/g·°C · ΔT = 22.0 − 62.0 = −40.0 °C
q = 100. g × 0.128 J1 g·°C × (−40.0 °C) = −512 J (answer B)

A subtracted the temperatures in the wrong order: 62.0 − 22.0 = +40.0 °C gives +512 J, heat absorbed by a cooling sinker. C stopped at m × c: 100. × 0.128 = 12.8 J, one degree's worth with no sign. D left out the mass: 0.128 × (−40.0) = −5.12 J, the heat for a single gram.

The sinker cooled 40 degrees, so it released heat: q must be negative. ✓
Dr. Karmach

Practice 3

q = m · c · ΔT
given: 45.0 g water · q = +2260 J · c = 4.184 J/g·°C · wanted: ΔT

45.0 g of water absorbs 2260 J of heat. By how much does its temperature rise, in °C? (c of water: 4.184 J/g·°C)

  1. 0.0833
  2. 50.2
  3. 12.0
  4. 210.
  5. 540.
Dr. Karmach

Practice 3 · answer: C

ΔT = q / (m · c)
given: 45.0 g water · q = +2260 J · c = 4.184 J/g·°C
ΔT = 2260 J45.0 g × 4.184 J/g·°C = +12.0 °C (answer C)

A flipped the rearrangement: 45.0 × 4.184 ÷ 2260 = 0.0833 °C. B left out c: 2260 ÷ 45.0 = 50.2 °C. D multiplied by c: 2260 × 4.184 ÷ 45.0 = 210. °C. E left out the mass: 2260 ÷ 4.184 = 540. °C, the change for a single gram.

Substitute back: 45.0 g × 4.184 J/g·°C × 12.0 °C = 2260 J. ✓
Dr. Karmach

Practice 4

q = m · c · ΔT
given: 25.0 g gold · Tinitial = 27.0 °C · absorbs 2.34 kJ · c = 0.129 J/g·°C · wanted: Tfinal

25.0 g of gold at 27.0 °C absorbs 2.34 kJ of heat. What is the final temperature, in °C? (c of gold: 0.129 J/g·°C)

  1. 27.7
  2. 699
  3. 726
  4. 753
  5. 39.1
Dr. Karmach

Practice 4 · answer: D

ΔT = q / (m · c), then Tfinal = Tinitial + ΔT
given: 25.0 g gold · Tinitial = 27.0 °C · q = +2340 J · c = 0.129 J/g·°C
ΔT = 2340 J25.0 g × 0.129 J/g·°C = +725.6 °C → Tfinal = 27.0 + 725.6 = 753 °C (answer D)

A left q in kilojoules: ΔT = 0.726 °C, so 27.7 °C. B subtracted Tinitial: 725.6 − 27.0 = 699 °C; Tfinal = Tinitial + ΔT. C stopped at ΔT: 726 °C is the change, not the final temperature. E multiplied by c: 2340 × 0.129 ÷ 25.0 = 12.07 °C, then 39.1 °C.

A tiny specific heat means a huge swing: over 700 degrees, most of the way to gold's 1064 °C melting point. ✓
Dr. Karmach

Practice 5

q = m · c · ΔT
given: 2.0 kg aluminum pan · 23.0 °C → 180.0 °C · c = 0.89 J/g·°C · wanted: q · the mass arrives in kilograms

A 2.0-kg aluminum pan heats from 23.0 °C to 180.0 °C on a burner. How much heat, in J, does the pan absorb? (c of aluminum: 0.89 J/g·°C)

  1. 280
  2. 1.8 × 10³
  3. 2.8 × 10⁵
  4. 3.2 × 10⁵
Dr. Karmach

Practice 5 · answer: C

q = m · c · ΔT
m = 2.0 kg = 2000 g · c = 0.89 J/g·°C · ΔT = 180.0 − 23.0 = +157.0 °C
q = 2.0 kg × 1000 g1 kg × 0.89 J1 g·°C × 157.0 °C = 279,460 J ≈ 2.8 × 10⁵ J (answer C)

c is per gram, so the kilograms convert inside the chain: 2.0 kg is 2000 g. A used 2.0 as if it were grams: 2.0 × 0.89 × 157.0 = 280 J, a thousand times short. B left out the temperature change: 2000 × 0.89 = 1.8 × 10³ J, one degree's worth. D used 180.0 as ΔT: 2000 × 0.89 × 180.0 = 3.2 × 10⁵ J. ΔT is final minus initial: 157.0 °C.

Two thousand grams climbing 157 degrees, even at aluminum's modest 0.89 J per gram per degree, costs about 280 kJ. ✓
Dr. Karmach

Check yourself

  1. Water cools from 50.0 °C to 20.0 °C. Write ΔT with its sign. What is the sign of q, and what does it say about the heat?
  2. Solve q = m·c·ΔT for m, in symbols. Which units cancel, and which unit survives?

Two samples can receive the same heat and change temperature by different amounts. Equal masses, equal q: the substance with the smaller specific heat shows the larger ΔT.

Dr. Karmach

4 · Comparing Specific Heats

For the same heat, read specific heat in reverse (equal masses, the smaller c means the larger temperature change; unequal masses, compare the whole sample's m·c), confirming with ΔT = q/mc when a number is wanted.

Dr. Karmach

The beach, twelve hours apart

At noon the sand scorches bare feet while the ocean stays cool. By midnight the sand is cold, and the water is the warm place to be.

Dr. Karmach

Silver spoon, porcelain cup

Specific heat, c: the heat that warms 1 g by 1 °C. Which has the higher c, the spoon or the cup?

Dr. Karmach

Silver spoon, porcelain cup

Specific heat, c: the heat that warms 1 g by 1 °C. Which has the higher c, the spoon or the cup?
The cup. Per gram, porcelain needs about four times the heat per degree.

silver: c = 0.235 J/g·°C · porcelain: c ≈ 1 J/g·°C
the same heat per gram swings the spoon's temperature about four times as far
Dr. Karmach

Same heat and mass: c and ΔT trade off

Give equal masses the same heat. Their temperature changes are not equal. Specific heat sits in the denominator of ΔT = q/mc, so the smaller c, the larger the temperature change.

ΔT = q / (m · c)
same q, same m: c in the denominator: smaller c, larger ΔT
Dr. Karmach

Ranking substances by specific heat

Every substance has its own specific heat; water's is several times any metal's. Higher c, smaller temperature change from the same heat.

water 4.184 · ethyl alcohol 2.46 · aluminum 0.897 · iron 0.449 · copper 0.385 · silver 0.235 · gold 0.129 · lead 0.128
specific heat c, in J/g·°C: smaller c, larger temperature change for the same heat and mass
Dr. Karmach

Why water resists temperature swings

Water soaks up heat with only a small temperature rise and releases it slowly, so coastlines stay mild. The cause is the strong grip between water molecules: hydrogen bonding.

2092 J into 100 g of each: water rises +5.0 °C · iron rises +46.6 °C
water's specific heat is 9.3× iron's, so the same heat moves it 9.3× less
Dr. Karmach

The method

  1. Compare the specific heats. Same heat and mass: smaller c means larger ΔT.
  2. Name the response. The substance with the smaller c swings more.
  3. Confirm with ΔT = q/mc. c and m are in the denominator.

Dr. Karmach

Guided example: water and gold

ΔT = q / (m · c)
10.0 g water (c = 4.184) and 10.0 g gold (c = 0.129) · q = 100. J each · wanted: each ΔT

10.0 g of water and 10.0 g of gold each absorb 100. J. Which changes temperature more, and by how much?

The masses are equal, so start with the specific heats.

Dr. Karmach

Guided example: solution

ΔT = q / (m · c)
10.0 g water (c = 4.184) · 10.0 g gold (c = 0.129) · q = 100. J each

Step 1 · Compare the specific heats

The masses are equal, so compare c alone. Gold's 0.129 is far smaller than water's 4.184.

Dr. Karmach

Guided example: solution

ΔT = q / (m · c)
10.0 g water (c = 4.184) · 10.0 g gold (c = 0.129) · q = 100. J each
Step 1 · Compare the specific heats Step 2 · Name the response

Smaller c, larger ΔT. Gold swings more.

Dr. Karmach

Guided example: solution

ΔT = q / (m · c)
10.0 g water (c = 4.184) · 10.0 g gold (c = 0.129) · q = 100. J each
Step 1 · Compare the specific heats Step 2 · Name the response Step 3 · Confirm with ΔT = q/mc
water: ΔT = 100. J10.0 g × 4.184 J/g·°C = +2.39 °C
gold: ΔT = 100. J10.0 g × 0.129 J/g·°C = +77.5 °C
Dr. Karmach

Guided example: solution

ΔT = q / (m · c)
10.0 g water (c = 4.184) · 10.0 g gold (c = 0.129) · q = 100. J each
Step 1 · Compare the specific heats Step 2 · Name the response Step 3 · Confirm with ΔT = q/mc
water: ΔT = 100. J10.0 g × 4.184 J/g·°C = +2.39 °C
gold: ΔT = 100. J10.0 g × 0.129 J/g·°C = +77.5 °C
Gold rises 77.5 °C, water only 2.39 °C. Water's c is 32 times gold's, so gold swings 32 times as far. ✓
Dr. Karmach

Guided example: the route on the strip

ΔT = q / (m · c)
given: 10.0 g water · 10.0 g gold · 100. J each · found: water +2.39 °C · gold +77.5 °C

Equal masses, so c alone decides which swings more. The equation confirms it. ✓
Dr. Karmach

Practice 1 · which ends hotter

ΔT = q / (m · c)
aluminum: c = 0.897 J/g·°C · silver: c = 0.235 J/g·°C

Equal masses of aluminum and silver start at 25 °C and absorb the same heat. Which ends hotter?

  1. Aluminum
  2. Silver
  3. Both end at the same temperature
  4. It depends on how much heat they absorb
Dr. Karmach

Practice 1 · answer: B

ΔT = q / (m · c) · equal masses, same heat: compare c
silver 0.235 · aluminum 0.897 J/g·°C · smaller c, larger ΔT

A read specific heat backwards: the larger c gives the smaller rise. C equal heat gives equal ΔT only when the specific heats match. D the heat sets how far each one warms, not which warms more: the smaller c wins at any heat.

Silver ends hotter. Its temperature swings about 3.8 times as far as aluminum's (0.897 / 0.235). ✓
Dr. Karmach

Practice 2 · one temperature change

ΔT = q / (m · c)
given: 30.0 g iron (c = 0.449) · 30.0 g aluminum (c = 0.897) · 450. J each

A 30.0 g iron bolt and a 30.0 g aluminum bolt each absorb 450. J. What is the iron bolt's temperature change, in °C?

  1. 16.7
  2. 6.74
  3. 15.0
  4. 33.4
Dr. Karmach

Practice 2 · answer: D

ΔT = q / (m · c)
iron: m = 30.0 g · c = 0.449 J/g·°C · q = 450. J
iron: ΔT = 450. J30.0 g × 0.449 J/g·°C = 450. J13.47 J/°C = +33.4 °C (answer D)

A used aluminum's c: 450. / (30.0 × 0.897) = 16.7. B multiplied by c instead of dividing: 450. × 0.449 / 30.0 = 6.74. C dropped c: 450. / 30.0 = 15.0.

Iron's c is half of aluminum's, so iron swings twice as far: 33.4 °C against 16.7 °C. ✓
Dr. Karmach

Practice 3 · ranking three substances

ΔT = q / (m · c)
given: iron c = 0.449 · ethyl alcohol c = 2.46 · copper c = 0.385 J/g·°C · equal masses · same heat

Equal masses of iron, ethyl alcohol and copper absorb the same heat. Rank them by ΔT, largest first.

  1. ethyl alcohol > iron > copper
  2. copper = iron > ethyl alcohol
  3. copper > iron > ethyl alcohol
  4. All three change by the same amount
Dr. Karmach

Practice 3 · answer: C

ΔT = q / (m · c) · equal masses, same heat: the smallest c swings most
copper 0.385 < iron 0.449 < ethyl alcohol 2.46 J/g·°C

A ranked by c itself: the largest c gives the smallest ΔT, not the largest. B lumped the metals together: copper's 0.385 sits below iron's 0.449, so copper still swings further. D equal heat gives equal ΔT only when the specific heats match.

Copper swings a little further than iron, and about 6.4 times as far as ethyl alcohol (2.46 / 0.385). ✓
Dr. Karmach

Worked example: when the masses differ

ΔT = q / (m · c)
200 g copper (c = 0.385) and 50.0 g aluminum (c = 0.897) · q = 2000 J each · wanted: which ends hotter

A 200 g copper block and a 50.0 g aluminum block each absorb 2000 J.

A common first answer: copper has the smaller specific heat, so copper wins. Check it: the masses are not equal.

Dr. Karmach

Worked example: solution

ΔT = q / (m · c)
200 g copper (c = 0.385) · 50.0 g aluminum (c = 0.897) · q = 2000 J each

Step 1 · Compare the specific heats

Copper's c, 0.385, is smaller than aluminum's, 0.897. But mass is in the denominator too, and the copper sample is four times heavier.

Dr. Karmach

Worked example: solution

ΔT = q / (m · c)
200 g copper (c = 0.385) · 50.0 g aluminum (c = 0.897) · q = 2000 J each
Step 1 · Compare the specific heats Step 2 · Name the response

Compare the whole sample's m·c: copper 200 × 0.385 = 77.0 J/°C, aluminum 50.0 × 0.897 = 44.85 J/°C. Aluminum's is smaller, so aluminum swings more.

Dr. Karmach

Worked example: solution

ΔT = q / (m · c)
200 g copper (c = 0.385) · 50.0 g aluminum (c = 0.897) · q = 2000 J each
Step 1 · Compare the specific heats Step 2 · Name the response Step 3 · Confirm with ΔT = q/mc
copper: ΔT = 2000 J200 g × 0.385 J/g·°C = 2000 J77.0 J/°C = +26.0 °C
aluminum: ΔT = 2000 J50.0 g × 0.897 J/g·°C = 2000 J44.85 J/°C = +44.6 °C
Dr. Karmach

Worked example: solution

ΔT = q / (m · c)
200 g copper (c = 0.385) · 50.0 g aluminum (c = 0.897) · q = 2000 J each
Step 1 · Compare the specific heats Step 2 · Name the response Step 3 · Confirm with ΔT = q/mc
copper: ΔT = 2000 J200 g × 0.385 J/g·°C = 2000 J77.0 J/°C = +26.0 °C
aluminum: ΔT = 2000 J50.0 g × 0.897 J/g·°C = 2000 J44.85 J/°C = +44.6 °C
Aluminum ends hotter, 44.6 °C against 26.0 °C, even though copper has the smaller specific heat. When the masses differ, compare m·c, not c alone. ✓
Dr. Karmach

Worked example: the route on the strip

ΔT = q / (m · c)
given: 200 g copper · 50.0 g aluminum · 2000 J each · found: copper +26.0 °C · aluminum +44.6 °C

Unequal masses, so compare m·c: aluminum's 44.85 J/°C is the smaller, so aluminum swings more. The equation confirms it. ✓
Dr. Karmach

Take-home: compare m·c, not c alone

200 g copper: m·c = 77.0 J/°C · 50.0 g aluminum: m·c = 44.85 J/°C
same 2000 J: copper +26.0 °C · aluminum +44.6 °C · the smaller m·c swings more

Comparing c alone assumes equal masses. When the masses differ, the whole sample's m·c sets the response: the smaller m·c, the larger the temperature change.

Dr. Karmach

Where this goes wrong

Equal heat, equal temperature. Equal q into equal mass does not give equal ΔT. 1000 J into 50.0 g of water raises it 4.78 °C; the same 1000 J into 50.0 g of copper raises it 51.9 °C. The specific heats differ, so the temperature changes differ.
Right substance, backwards reason. Naming the low-c substance as the one that ends hotter "because it stores more heat per gram." It stores less per gram: lead takes 0.128 J to warm a gram by a degree, aluminum 0.897 J. That low cost per degree is exactly why lead swings more.
Comparing c when the masses differ. The rule "smaller c wins" assumes equal mass. When the masses are not equal, mass is in the denominator too. Compare the whole sample's m·c, or run ΔT = q/mc for each.
Dr. Karmach

Practice 4

ΔT = q / (m · c)
given: 400. g lead (c = 0.128) · 150. g silver (c = 0.235) · 1200 J each · same start

A 400. g block of lead (c = 0.128 J/g·°C) and a 150. g block of silver (c = 0.235 J/g·°C) start at the same temperature and each absorb 1200 J. Which statement matches the outcome?

  1. Lead warms by about 23.4 °C and silver by about 34.0 °C, so silver ends hotter.
  2. Lead ends hotter: its smaller specific heat turns the same heat into the larger rise.
  3. Both warm by the same amount, since each absorbs the same 1200 J.
  4. Lead warms by about 34.0 °C and silver by about 23.4 °C, so lead ends hotter.
Dr. Karmach

Practice 4 · answer: A

ΔT = q / (m · c) · the masses differ, so compare m·c
lead: 400. × 0.128 = 51.2 J/°C · silver: 150. × 0.235 = 35.25 J/°C · silver's is smaller
lead: ΔT = 1200 J51.2 J/°C = +23.4 °C · silver: ΔT = 1200 J35.25 J/°C = +34.0 °C (answer A)

B compared c alone: "smaller c wins" holds only at equal masses, and the lead block is heavier. C equal heat does not mean equal ΔT: the two samples' m·c differ. D computed both rises and pinned them on the wrong metals.

Silver has the larger c, yet its smaller m·c makes it swing more: 34.0 °C against 23.4 °C. ✓
Dr. Karmach

Extra practice 1

ΔT = q / (m · c)
lead: c = 0.128 J/g·°C · copper: c = 0.385 J/g·°C · equal masses · same heat

Two blocks of equal mass, one lead and one copper, take in the same heat. The lead warms by 36.0 °C. By how much, in °C, does the copper warm?

  1. 36.0
  2. 12.0
  3. 108
  4. 4.61
Dr. Karmach

Extra practice 1 · answer: B

ΔT = q / (m · c) · equal masses, same heat: c alone decides
lead 0.128 · copper 0.385 J/g·°C · copper's c is larger, so copper warms less
q/m = 0.128 × 36.0 = 4.61 J/g  →  copper: ΔT = 4.61 J/g0.385 J/g·°C = +12.0 °C · answer B

A took equal heat as an equal rise: 36.0 °C holds only when the specific heats match. C flipped the ratio: 36.0 × 0.385 / 0.128 = 108, but the larger c gives the smaller rise. D stopped halfway: 0.128 × 36.0 = 4.61 is the heat per gram, in J/g, not copper's rise.

Copper's c is 3.0 times lead's (0.385 / 0.128), so copper warms a third as far: 36.0 / 3.0 = 12.0 °C. ✓
Dr. Karmach

Extra practice 2

q = m · c · ΔT
silver: c = 0.235 J/g·°C · iron: c = 0.449 J/g·°C · 1 cal = 4.184 J

A silver bar and an iron bar, 60.0 g each, both warm by 25.0 °C. How much more heat, in cal, does the iron bar absorb?

  1. 76.7
  2. 321
  3. 1.34 × 10³
  4. 161
Dr. Karmach

Extra practice 2 · answer: A

q = m · c · ΔT · same m and ΔT: the larger c takes more heat
60.0 g each · +25.0 °C each · iron 0.449 · silver 0.235 J/g·°C · 1 cal = 4.184 J
iron: 60.0 × 0.449 × 25.0 = 673.5 J  ·  silver: 60.0 × 0.235 × 25.0 = 352.5 J
673.5 J − 352.5 J = 321 J × 1 cal4.184 J = 76.7 cal · answer A

B stopped in joules: 321 J is the right gap in the wrong unit. C put the factor upside down: 321 × 4.184 = 1.34 × 10³. D never subtracted silver's heat: 673.5 / 4.184 = 161 cal is iron's whole heat.

Iron's c beats silver's by 0.214 J/g·°C. Over 60.0 g and 25.0 °C that is 321 J, about 77 cal. ✓
Dr. Karmach

Extra practice 3

ΔT = q / (m · c), then Tfinal = Tinitial + ΔT
iron: c = 0.449 J/g·°C · aluminum: c = 0.897 J/g·°C

A 140. g iron block at 30.0 °C and a 40.0 g aluminum block at 22.0 °C each absorb 1500. J. Which statement matches the outcome?

  1. Iron ends hotter: it starts warmer, and the same heat gives the same rise.
  2. Iron ends hotter, at 53.9 °C: its smaller specific heat gives the larger rise.
  3. Aluminum ends hotter, at 41.8 °C.
  4. Aluminum ends hotter, at 63.8 °C.
Dr. Karmach

Extra practice 3 · answer: D

ΔT = q / (m · c) · the masses differ, so compare m·c
iron: 140. × 0.449 = 62.86 J/°C · aluminum: 40.0 × 0.897 = 35.88 J/°C · 1500. J each
iron: ΔT = 1500. J62.86 J/°C = +23.9 °C  →  30.0 °C + 23.9 °C = 53.9 °C
aluminum: ΔT = 1500. J35.88 J/°C = +41.8 °C  →  22.0 °C + 41.8 °C = 63.8 °C · answer D

A took equal heat as an equal rise: that holds only when m·c matches, and 62.86 is not 35.88. B compared c alone: iron's 140. g makes its m·c the larger, so it rises only 23.9 °C. C stopped at the rise: 41.8 °C is how far aluminum climbs from 22.0 °C, not where it ends.

Aluminum starts 8.0 °C cooler but climbs about 18 °C further, so it finishes about 10 °C ahead. ✓
Dr. Karmach

Check yourself

  1. Equal masses of copper and water absorb the same heat from the same start. Which ends hotter, and which term in ΔT = q/mc decides it?
  2. Two iron bars, 50 g and 150 g, absorb the same heat. Which shows the larger temperature change, and why?
Dr. Karmach

5 · Calorimetry

Use an insulated cup to make energy conservation visible (the heat one body loses equals the heat another gains) and solve for the heat a metal or a reaction in solution gives off, a final temperature, an unknown specific heat, or a food's Calories per gram, with any final temperature landing between the two starting temperatures.

Dr. Karmach

How a Calorie gets measured

A food label's Calorie number is not estimated. The food is burned in a sealed chamber, water around it absorbs the heat, and the temperature rise gives the count.

Dr. Karmach

Heat lost equals heat gained

Nest two foam cups, add a lid and a thermometer, and almost no heat escapes. Whatever heat the hot object loses, the water gains. The two settle at one shared temperature.

Dr. Karmach

Energy is conserved in the cup

Inside the insulated cup, the energy that leaves one body enters the other. Energy is conserved: none is created or destroyed.

qA + qB = 0 → qA = −qB
each body: q = m·c·ΔT with ΔT = Tf − Ti · one q comes out negative: that body released the heat
Dr. Karmach

The final temperature sits between

Both bodies end at the same temperature. It lands between the two starting temperatures, pulled toward whichever body carries the larger m·c: usually the water.

Dr. Karmach

The method

  1. Set the balance: qA = −qB, ΔT = Tf − Ti each.
  2. Solve without expanding: Tf = the m·c-weighted average.
  3. Check: Tf between the starts; heat lost = heat gained.
Dr. Karmach

Every route starts from the water

The water's mass and ΔT give qwater. One sign flip gives the heat of the metal, reaction, or burning food in it. Two mixed solutions: add their volumes for the mass.

Dr. Karmach

Guided example: a hot copper pipe

qmetal + qwater = 0 → qmetal = −qwater
given: 72.5 g copper pipe, heated · 150.0 g water at 21.0 °C · final 33.6 °C · wanted: q of the pipe

A heated 72.5 g copper pipe goes into a calorimeter holding 150.0 g of water at 21.0 °C. Both settle at 33.6 °C. Find q for the pipe. Did the pipe gain or lose heat?

Start with the water: its mass and both temperatures are known.

Dr. Karmach

Guided example: solution

qmetal = −qwater
150.0 g water · ΔT = 33.6 − 21.0 = +12.6 °C · the pipe's starting temperature was never measured

Step 1 · Set the balance

The water's numbers are complete, so its q comes first. The pipe's q is the same amount with the opposite sign.

Dr. Karmach

Guided example: solution

qmetal = −qwater
150.0 g water · ΔT = 33.6 − 21.0 = +12.6 °C · the pipe's starting temperature was never measured
Step 1 · Set the balance Heat gained by the water
qwater = 150.0 g × 4.184 J/g·°C × 12.6 °C = +7.91 × 10³ J
Dr. Karmach

Guided example: solution

qmetal = −qwater
150.0 g water · ΔT = 33.6 − 21.0 = +12.6 °C · the pipe's starting temperature was never measured
Step 1 · Set the balance Heat gained by the water
qwater = 150.0 g × 4.184 J/g·°C × 12.6 °C = +7.91 × 10³ J
Flip the sign
qpipe = −qwater = −7.91 × 10³ J
Dr. Karmach

Guided example: solution

qmetal = −qwater
150.0 g water · ΔT = 33.6 − 21.0 = +12.6 °C · the pipe's starting temperature was never measured
Step 1 · Set the balance Heat gained by the water
qwater = 150.0 g × 4.184 J/g·°C × 12.6 °C = +7.91 × 10³ J
Flip the sign
qpipe = −qwater = −7.91 × 10³ J
The water warmed, so the pipe lost heat: its q is negative. The pipe's 72.5 g never entered; the water alone measured the heat. ✓
Dr. Karmach

Guided example: the route on the map

qmetal = −qwater
given: 150.0 g water, 21.0 → 33.6 °C · found: qpipe = −7.91 × 10³ J

Two moves: q = m·c·ΔT for the water, then the sign flip. ✓
Dr. Karmach

Worked example 1: mixing hot and cold water

qhot = −qcold · ΔT = Tf − Ti on both sides
given: 150 g water at 70 °C · 100 g water at 20 °C · wanted: Tf

Pour 150 g of water at 70 °C into 100 g at 20 °C. Both are water, so both specific heats are 4.184. Find the final temperature.

Dr. Karmach

Worked example 1: solution

qhot = −qcold · ΔT = Tf − Ti on both sides
150 g water at 70 °C · 100 g water at 20 °C · same c = 4.184, cancels

Step 1 · Set the balance

Each body keeps its own ΔT = Tf − Ti: 150 · (Tf − 70) = −100 · (Tf − 20). The hot side's ΔT will come out negative; the minus sign hands its released heat to the cold side.

Dr. Karmach

Worked example 1: solution

qhot = −qcold · ΔT = Tf − Ti on both sides
150 g water at 70 °C · 100 g water at 20 °C · same c = 4.184, cancels
Step 1 · Set the balance Step 2 · Solve without expanding
Tf = 150 × 70 + 100 × 20150 + 100 = 12,500250 = 50.0 °C

The balance point is the mass-weighted average of the two starting temperatures. No distributing, no collecting terms: the masses weight the two starts directly.

Dr. Karmach

Worked example 1: solution

qhot = −qcold · ΔT = Tf − Ti on both sides
150 g water at 70 °C · 100 g water at 20 °C · same c = 4.184, cancels
Step 1 · Set the balance Step 2 · Solve without expanding
Tf = 150 × 70 + 100 × 20150 + 100 = 12,500250 = 50.0 °C
Step 3 · Check
50.0 °C lands between 20 and 70, closer to 70 because the hotter sample is heavier. And the books balance: the hot water released 150 × 4.184 × 20.0 = 12,552 J, the cold water absorbed 100 × 4.184 × 30.0 = 12,552 J. Heat lost = heat gained. ✓
Dr. Karmach

Worked example 1: the route on the map

qhot = −qcold
given: 150 g water at 70 °C · 100 g water at 20 °C · found: Tf = 50.0 °C

With Tf unknown, neither q can come first. One move, the m·c-weighted average, gives Tf directly. ✓
Dr. Karmach

Worked example 2: a hot bolt in water

qiron = −qwater · ΔT = Tf − Ti on both sides
given: 100 g iron at 90 °C · 150 g water at 20 °C · c: iron 0.449, water 4.184 · wanted: Tf

A 100 g iron bolt at 90 °C drops into 150 g of water at 20 °C.

A common first attempt: add the two heats. Test the result against the thermometer.

Dr. Karmach

Worked example 2: solution

qiron = −qwater · ΔT = Tf − Ti on both sides
100 g iron at 90 °C · 150 g water at 20 °C

A common first attempt

adding the heats: Tf = 14.6 °C ✗
14.6 °C is below both 20 °C and 90 °C: no shared temperature sits outside the pair

Same signs on both heats is the slip. One body loses, the other gains.

Dr. Karmach

Worked example 2: solution

qiron = −qwater · ΔT = Tf − Ti on both sides
100 g iron at 90 °C · 150 g water at 20 °C
A common first attempt
adding the heats: Tf = 14.6 °C ✗
14.6 °C is below both 20 °C and 90 °C: no shared temperature sits outside the pair
Step 1 · Set the balance
44.9 × (Tf − 90) = −627.6 × (Tf − 20)
The two m·c terms are set: iron's 100 × 0.449 = 44.9 against the water's 150 × 4.184 = 627.6, each with its own Tf − Ti. The iron's ΔT will come out negative. ✓
Dr. Karmach

Worked example 2: the final temperature

qiron = −qwater · ΔT = Tf − Ti on both sides
m·c: iron 44.9, water 627.6 · start 90 °C and 20 °C

Step 2 · Solve without expanding

Tf = 44.9 × 90 + 627.6 × 2044.9 + 627.6 = 24.7 °C
24.7 °C sits between 20 and 90, close to the water: its m·c of 627.6 dwarfs the iron's 44.9. ✓
Dr. Karmach

Worked example 2: the route on the map

qiron = −qwater
given: 100 g iron at 90 °C · 150 g water at 20 °C · found: Tf = 24.7 °C

The same one move as two water samples. Only the m·c weights changed. ✓
Dr. Karmach

Take-home: one loses, the other gains

heat lost by the hot body = heat gained by the cold body
Tf always lands between the two starting temperatures

Never add the two heats. One body releases, the other absorbs. Set the loss equal to the gain, and a final temperature outside the starting pair means a dropped sign.

Dr. Karmach

Your turn: aluminum into water

Drop 80 g aluminum (c = 0.897) at 100 °C into 200 g water at 22 °C. Fill the m·c terms into the weighted average that solves qAl = −qwater.

Tf = × 100 + × 22 + = °C
Dr. Karmach

Your turn: aluminum into water

Drop 80 g aluminum (c = 0.897) at 100 °C into 200 g water at 22 °C. Fill the m·c terms into the weighted average that solves qAl = −qwater.

Tf = × 100 + × 22 + = °C
Tf = 71.76 × 100 + 836.8 × 2271.76 + 836.8 = 28.2 °C
Between 22 and 100, and close to 22: the water's m·c of 836.8 far outweighs the aluminum's 71.76. ✓
Dr. Karmach

The bomb calorimeter: the water does the measuring

qfood = −qwater · qwater = m·c·ΔT
water's mass from its volume at 1.00 g/mL · kJ ÷ grams burned = kJ/g · 1 Cal = 4.184 kJ

Food burns in a sealed steel chamber sunk in water. The water absorbs all the heat, so its temperature rise measures it. Divide by the grams burned for the energy per gram.

Dr. Karmach

Worked example 3: Calories per gram of a candy bar

qfood = −qwater · qwater = m·c·ΔT
given: 5.00 g of candy bar burned · 1840 mL water · 20.0 → 35.0 °C · wanted: heat released per gram, in kJ/g and Cal/g

A 5.00 g piece of a candy bar burns in a bomb calorimeter holding 1840 mL of water. The water warms from 20.0 to 35.0 °C. Find the heat released per gram, in kJ/g and in Cal/g.

Dr. Karmach

Worked example 3: solution

qfood = −qwater · qwater = m·c·ΔT
5.00 g burned · 1840 mL water = 1840 g at 1.00 g/mL · ΔT = 35.0 − 20.0 = +15.0 °C

Two moves are needed.

Step 1 · Heat gained by the water

qwater = 1840 g × 4.184 J/g·°C × 15.0 °C = 115,478 J = 1.15 × 10⁵ J

The water gained 1.15 × 10⁵ J, so the burning food released it: qfood = −1.15 × 10⁵ J.

Dr. Karmach

Worked example 3: solution

qfood = −qwater · qwater = m·c·ΔT
5.00 g burned · 1840 mL water = 1840 g at 1.00 g/mL · ΔT = 35.0 − 20.0 = +15.0 °C
Two moves are needed. Step 1 · Heat gained by the water
qwater = 1840 g × 4.184 J/g·°C × 15.0 °C = 115,478 J = 1.15 × 10⁵ J
Step 2 · Per gram, then Calories
115.5 kJ5.00 g = 23.1 kJ/g → 23.1 kJ/g × 1 Cal4.184 kJ = 5.52 Cal/g
A 40.0 g bar of it releases 40.0 g × 5.52 Cal/g = 221 Cal. Fat carries about 9 Cal/g and sugar about 4, so a bar of both lands near 5.5. ✓
Dr. Karmach

Worked example 3: the route on the map

qfood = −qwater
given: 5.00 g burned · 1840 g water, 20.0 → 35.0 °C · found: 23.1 kJ/g = 5.52 Cal/g

Step 1 of the solution is arrows 1 and 2: the water's q, then the sign flip. Step 2 is arrows 3 and 4. ✓
Dr. Karmach

Where this goes wrong

100 g iron at 90 °C into 150 g water at 20 °C → Tf = 24.7 °C
the correct final temperature both bodies reach
Ignoring the water's share. Assuming the metal just cools to the water's temperature gives Tf = 20 °C. The water warms too; its gain is part of the balance.
Adding the two heats. Same sign on both sides gives Tf = 14.6 °C, below both starting temperatures. One body loses heat, the other gains it: heat lost = heat gained.
Swapping the masses onto the wrong specific heats. Pairing 150 with the iron and 100 with the water gives Tf = 29.7 °C. Each mass keeps its own substance's c.
Dr. Karmach

Practice 1

qmetal = −qwater
given: 45.0 g iron bearing, hot · 110.0 g water at 19.5 °C · both end at 30.8 °C · c: iron 0.449, water 4.184 · wanted: q of the bearing

A 45.0 g iron bearing, hot from a grinder, drops into 110.0 g of water at 19.5 °C. The water warms to 30.8 °C. What is q for the bearing, in joules?

  1. −2.13 × 10³
  2. 5.20 × 10³
  3. −558
  4. −5.20 × 10³
Dr. Karmach

Practice 1 · answer: D

qmetal = −qwater
110.0 g water · ΔT = 30.8 − 19.5 = +11.3 °C · the bearing's own ΔT is unknown
qwater = 110.0 g × 4.184 J/g·°C × 11.3 °C = +5.20 × 10³ J → qbearing = −5.20 × 10³ J (answer D)

A put the bearing's 45.0 g into the water's q: −(45.0 × 4.184 × 11.3) = −2.13 × 10³. B stopped at qwater: +5.20 × 10³ is the heat the water gained, before the sign flip. C used iron's specific heat for the water: −(110.0 × 0.449 × 11.3) = −558.

The water warmed, so the bearing lost heat: q is negative, and it matches the water's gain in size. ✓
Dr. Karmach

Practice 2

qreaction = −qsolution
given: 60.0 mL acid + 60.0 mL base, both at 20.8 °C · peak 33.9 °C · treat as water: 1.00 g/mL, c = 4.184

In a coffee-cup calorimeter, 60.0 mL of hydrochloric acid and 60.0 mL of sodium hydroxide solution, both at 20.8 °C, are mixed. The temperature peaks at 33.9 °C. What is q for the reaction, in joules?

  1. −6.58 × 10³
  2. −3.29 × 10³
  3. 6.58 × 10³
  4. −1.70 × 10⁴
Dr. Karmach

Practice 2 · answer: A

qreaction = −qsolution
60.0 mL + 60.0 mL = 120.0 mL = 120.0 g at 1.00 g/mL · ΔT = 33.9 − 20.8 = +13.1 °C
qsolution = 120.0 g × 4.184 J/g·°C × 13.1 °C = +6.58 × 10³ J → qreaction = −6.58 × 10³ J (answer A)

B counted one solution's 60.0 g: the whole 120.0 g mixture warmed, so −(60.0 × 4.184 × 13.1) = −3.29 × 10³ is half the heat. C stopped at qsolution: +6.58 × 10³, before the sign flip. D used the peak temperature as ΔT: −(120.0 × 4.184 × 33.9) = −1.70 × 10⁴.

The mixture warmed, so the reaction released heat: qreaction is negative, exothermic. ✓
Dr. Karmach

Practice 2: the route on the map

qreaction = −qsolution
given: 60.0 mL + 60.0 mL mixed, 20.8 → 33.9 °C · found: qreaction = −6.58 × 10³ J

The whole 120.0 g mixture is the water; flip its q for the reaction. ✓
Dr. Karmach

Practice 3

heat lost = heat gained
given: 60.0 g copper at 120.0 °C · 125 g water at 25.0 °C · c: copper 0.385, water 4.184 · wanted: Tf

A 60.0 g copper block at 120.0 °C drops into 125 g of water at 25.0 °C. What final temperature, in °C, do they reach?

  1. 29.0
  2. 40.3
  3. 55.8
  4. 72.5
Dr. Karmach

Practice 3 · answer: A

heat lost = heat gained
m·c: copper 60.0 × 0.385 = 23.1 · water 125 × 4.184 = 523 · start 120.0 °C and 25.0 °C
Tf = 23.1 × 120.0 + 523 × 25.023.1 + 523 = 29.0 °C (answer A)

B swapped the masses onto the wrong specific heats: 40.3 °C. C dropped the specific heats and weighted by mass alone: (60.0 × 120.0 + 125 × 25.0) ÷ 185 = 55.8 °C, a shortcut that works only when both bodies are water. D took the plain average of the starts: (120.0 + 25.0) ÷ 2 = 72.5 °C, as if the two bodies weighed the same and shared one c.

29.0 °C sits between 25 and 120, close to the water: its m·c of 523 outweighs the copper's 23.1. ✓
Dr. Karmach

Practice 4

qmetal = −qwater · ΔT = Tf − Ti on both sides
given: 95.0 g metal at 99.0 °C · 40.0 g water at 18.0 °C · measured: Tf = 34.5 °C · wanted: c of the metal

A 95.0 g sample of an unknown metal at 99.0 °C drops into 40.0 g of water at 18.0 °C. Both settle at 34.5 °C. What is the metal's specific heat, in J/g·°C?

  1. −0.451
  2. 2.76 × 10³
  3. 0.843
  4. 0.451
  5. 2.54
Dr. Karmach

Practice 4 · answer: D

qmetal = −qwater · ΔT = Tf − Ti on both sides
water: 40.0 g · ΔT = 34.5 − 18.0 = +16.5 °C · metal: 95.0 g · ΔT = 34.5 − 99.0 = −64.5 °C
qwater = 40.0 g × 4.184 J/g·°C × 16.5 °C = 2761 J → c = −2761 J95.0 g × (−64.5 °C) = 0.451 J/g·°C (answer D)

A dropped the minus in qmetal = −qwater: 2761 ÷ (95.0 × (−64.5)) = −0.451, a negative specific heat. B stopped at qwater: 2761 J, before dividing by the metal's m·ΔT. C used the final temperature as the metal's ΔT: 2761 ÷ (95.0 × 34.5) = 0.843. E swapped the two masses: −(95.0 × 4.184 × 16.5) ÷ (40.0 × (−64.5)) = 2.54.

The metal fell 64.5 °C while the water rose only 16.5 °C: the metal's m·c, 95.0 × 0.451 = 42.8, is about a quarter of the water's 167. A c near 0.45, like iron's, fits. ✓
Dr. Karmach

Practice 5

qfood = −qwater · qwater = m·c·ΔT
given: 52.7 g granola bar · 4.00 g of it burned · 1650 mL water · 20.5 → 32.1 °C · wanted: Calories released by the whole bar

A food lab burns a 4.00 g chip of a 52.7 g granola bar in a bomb calorimeter. The 1650 mL water jacket climbs from 20.5 to 32.1 °C. How many Calories does the whole bar release?

  1. 252
  2. 4.41 × 10³
  3. 19.1
  4. 698
  5. 1.06 × 10³
Dr. Karmach

Practice 5 · answer: A

qfood = −qwater · qwater = m·c·ΔT
1650 mL water = 1650 g · ΔT = 32.1 − 20.5 = +11.6 °C · 4.00 g burned · whole bar 52.7 g
qwater = 1650 g × 4.184 J/g·°C × 11.6 °C = 80,082 J → 80.08 kJ4.00 g = 20.0 kJ/g
52.7 g × 20.0 kJ1 g × 1 Cal4.184 kJ = 252 Cal (answer A)

B multiplied by 4.184: 1055 × 4.184 = 4.41 × 10³. C skipped the scale-up: 80.08 kJ ÷ 4.184 = 19.1, the chip alone. D used 32.1 °C as ΔT: 698. E stopped at kilojoules: 1.06 × 10³.

252 Cal for a 52.7 g bar is about 4.8 Cal/g, between sugar's 4 and fat's 9, where a granola bar sits. ✓
Dr. Karmach

Check yourself

  1. A hot metal is dropped into cool water in an insulated cup. Write the conservation law that relates the heat the metal loses to the heat the water gains.
  2. A final temperature comes out below both starting temperatures. What went wrong, and what does the correct answer always sit between?

A reaction releases a fixed amount of heat per mole, and the calorimeter is how that number gets measured. Written beside its balanced equation as ΔH, it becomes a conversion factor as real as any molar mass.

Dr. Karmach

6 · Thermochemical Equations

Treat ΔH as tied to the equation as written: reverse the equation and flip its sign, scale the coefficients and scale ΔH in step, and use ΔH as a conversion factor to find the heat released or absorbed by a given amount of substance.

Dr. Karmach

The gas bill charges for heat

The utility charges for energy delivered, not the gas itself. Burning a set amount of fuel releases a set amount of heat, and the bill counts that heat.

Dr. Karmach

ΔH is tied to the equation as written

A thermochemical equation pairs a balanced equation with its ΔH. That ΔH belongs to those exact coefficients and states. Change the equation, and ΔH changes with it.

CH₄(g) + 2 O₂(g) → CO₂(g) + 2 H₂O(l) · ΔH = −890 kJ
−890 kJ is released when 1 mol CH₄ burns exactly as written
Dr. Karmach

Reverse the equation, flip the sign

Running a reaction backward reverses its heat flow. A release becomes an equal absorption. The magnitude is unchanged; only the sign flips.

H₂O(l) → H₂(g) + ½ O₂(g) · ΔH = +286 kJ
forward, ΔH = −286 kJ (released) · reversed, ΔH = +286 kJ (absorbed)
Dr. Karmach

Scale the coefficients, scale ΔH

ΔH is proportional to the amount reacting. Double every coefficient and twice as much reacts, so ΔH doubles. Halve them and ΔH halves.

2 H₂(g) + O₂(g) → 2 H₂O(l) · ΔH = −572 kJ
from H₂ + ½ O₂ → H₂O, ΔH = −286 kJ, scaled ×2
Dr. Karmach

ΔH is a conversion factor

The coefficients turn ΔH into a factor: kJ per mole of any species in the equation. Chain it with molar mass to move between grams of fuel and kilojoules of heat.

Dr. Karmach

The method

  1. Match the target to the given. Reverse the equation if the target runs backward.
  2. Flip the sign for a reversal; scale ΔH by the factor that scales the coefficients.
  3. For heat, use ΔH as kJ per mole and cancel units.
Dr. Karmach

Worked example 1: reversing an equation

C(s) + O₂(g) → CO₂(g) · ΔH = −394 kJ
given: this equation and ΔH · wanted: ΔH for the reverse

Carbon burns to carbon dioxide, releasing 394 kJ. What is ΔH for the reverse, CO₂(g) → C(s) + O₂(g)?

Dr. Karmach

Worked example 1: solution

C(s) + O₂(g) → CO₂(g) · ΔH = −394 kJ
forward: 394 kJ released

Step 1 · Match the target to the given

The target runs the other way: CO₂ breaks apart into C and O₂. It is the reverse.

Dr. Karmach

Worked example 1: solution

C(s) + O₂(g) → CO₂(g) · ΔH = −394 kJ
forward: 394 kJ released
Step 1 · Match the target to the given Step 2 · Flip the sign
CO₂(g) → C(s) + O₂(g) · ΔH = +394 kJ
−394 kJ released → +394 kJ absorbed · same magnitude, opposite sign
Splitting CO₂ must cost exactly the energy its formation released. ✓
Dr. Karmach

Worked example 2: reverse and scale

H₂(g) + ½ O₂(g) → H₂O(l) · ΔH = −286 kJ
given: this equation and ΔH · wanted: ΔH for 2 H₂O(l) → 2 H₂(g) + O₂(g)

Find ΔH for 2 H₂O(l) → 2 H₂(g) + O₂(g).

A common first attempt: flip the sign but leave the coefficients' change out of ΔH. Test it.

Dr. Karmach

Worked example 2: solution

H₂(g) + ½ O₂(g) → H₂O(l) · ΔH = −286 kJ
target: 2 H₂O(l) → 2 H₂(g) + O₂(g)

Step 1 · Match the target to the given

The target is reversed and every coefficient is doubled. Two changes, so ΔH takes two steps.

Dr. Karmach

Worked example 2: solution

H₂(g) + ½ O₂(g) → H₂O(l) · ΔH = −286 kJ
target: 2 H₂O(l) → 2 H₂(g) + O₂(g)
Step 1 · Match the target to the given Step 2 · Flip the sign, then scale ΔH
ΔH = −(2 × −286 kJ) = +572 kJ
Flip only: +286 kJ ✗. Scale only: −572 kJ ✗. Both moves give +572 kJ: forming 2 mol water released 572 kJ, so splitting it absorbs 572 kJ. ✓
Dr. Karmach

Take-home: reverse flips, scale multiplies

flip the arrow, flip the sign · scale the equation, scale the ΔH
reversed: ΔH × (−1) · scaled by n: ΔH × n · do both when both apply

Each change to the equation changes ΔH. Reversing flips the sign. Scaling multiplies. A target that is both reversed and doubled needs both moves. Say the rule until it is automatic.

Dr. Karmach

Your turn: reverse and scale

Given 2 SO₂(g) + O₂(g) → 2 SO₃(g), ΔH = −198.2 kJ, find ΔH for 4 SO₃(g) → 4 SO₂(g) + 2 O₂(g) (reversed and doubled).

ΔH = ( × −198.2 kJ) = kJ
Dr. Karmach

Your turn: reverse and scale

Given 2 SO₂(g) + O₂(g) → 2 SO₃(g), ΔH = −198.2 kJ, find ΔH for 4 SO₃(g) → 4 SO₂(g) + 2 O₂(g) (reversed and doubled).

ΔH = ( × −198.2 kJ) = kJ
ΔH = −(2 × −198.2 kJ) = +396.4 kJ
Reversed, so the sign flips; doubled, so ×2. Forming 4 mol SO₃ released 396.4 kJ, so the reverse absorbs it. ✓
Dr. Karmach

Reading ΔH per mole of each substance

CH₄(g) + 2 O₂(g) → CO₂(g) + 2 H₂O(l) · ΔH = −890 kJ
−890 kJ goes with 1 mol CH₄ · with 2 mol O₂ · with 1 mol CO₂ · with 2 mol H₂O

Pick one substance. Its coefficient, in moles, goes under ΔH, either way up.

−890 kJ1 mol CH₄ or 1 mol CH₄−890 kJ · −890 kJ2 mol O₂ or 2 mol O₂−890 kJ

Subscripts never enter the factor. The 2 in O₂ counts atoms inside one molecule.

Dr. Karmach

Guided example: a camping stove

C₃H₈(g) + 5 O₂(g) → 3 CO₂(g) + 4 H₂O(l) · ΔH = −2220 kJ
given: 0.250 mol C₃H₈ · wanted: ΔH in kJ

A camping stove burns 0.250 mol of propane. What is ΔH for this amount?

Read the equation first: burning 1 mol C₃H₈ releases 2220 kJ.

Dr. Karmach

Guided example: solution

C₃H₈(g) + 5 O₂(g) → 3 CO₂(g) + 4 H₂O(l) · ΔH = −2220 kJ
given: 0.250 mol C₃H₈ · −2220 kJ per 1 mol C₃H₈

Step 1 · Write ΔH per mole of C₃H₈

Propane's coefficient is 1: −2220 kJ per 1 mol C₃H₈. As a recipe, 0.250 mol is a quarter of a mole, so it releases a quarter of the heat.

Dr. Karmach

Guided example: solution

C₃H₈(g) + 5 O₂(g) → 3 CO₂(g) + 4 H₂O(l) · ΔH = −2220 kJ
given: 0.250 mol C₃H₈ · −2220 kJ per 1 mol C₃H₈
Step 1 · Write ΔH per mole of C₃H₈ Step 2 · Cancel mol C₃H₈
0.250 mol C₃H₈ × −2220 kJ1 mol C₃H₈ = −555 kJ
Dr. Karmach

Guided example: solution

C₃H₈(g) + 5 O₂(g) → 3 CO₂(g) + 4 H₂O(l) · ΔH = −2220 kJ
given: 0.250 mol C₃H₈ · −2220 kJ per 1 mol C₃H₈
Step 1 · Write ΔH per mole of C₃H₈ Step 2 · Cancel mol C₃H₈
0.250 mol C₃H₈ × −2220 kJ1 mol C₃H₈ = −555 kJ
A quarter of 2220 kJ is 555 kJ, released, so ΔH is negative. The conversion factor and the recipe agree. ✓
Dr. Karmach

Guided example: counted from the oxygen

C₃H₈(g) + 5 O₂(g) → 3 CO₂(g) + 4 H₂O(l) · ΔH = −2220 kJ
0.250 mol C₃H₈ burns with 0.250 × 5 = 1.25 mol O₂ · −2220 kJ per 5 mol O₂

Write ΔH per mole of O₂

Oxygen's coefficient is 5, so 5 mol O₂ goes under ΔH.

Dr. Karmach

Guided example: counted from the oxygen

C₃H₈(g) + 5 O₂(g) → 3 CO₂(g) + 4 H₂O(l) · ΔH = −2220 kJ
0.250 mol C₃H₈ burns with 0.250 × 5 = 1.25 mol O₂ · −2220 kJ per 5 mol O₂
Write ΔH per mole of O₂ Cancel mol O₂
1.25 mol O₂ × −2220 kJ5 mol O₂ = −555 kJ
Dr. Karmach

Guided example: counted from the oxygen

C₃H₈(g) + 5 O₂(g) → 3 CO₂(g) + 4 H₂O(l) · ΔH = −2220 kJ
0.250 mol C₃H₈ burns with 0.250 × 5 = 1.25 mol O₂ · −2220 kJ per 5 mol O₂
Write ΔH per mole of O₂ Cancel mol O₂
1.25 mol O₂ × −2220 kJ5 mol O₂ = −555 kJ
Same heat as the propane count. Keeping −2220 kJ per 1 mol O₂ gives 1.25 × −2220 = −2775 kJ, five times too much. ✓
Dr. Karmach

Guided example: the route on the map

C₃H₈(g) + 5 O₂(g) → 3 CO₂(g) + 4 H₂O(l) · ΔH = −2220 kJ
given: 0.250 mol C₃H₈ · found: −555 kJ

Moles in hand: one arrow, one conversion factor, ΔH per mole of C₃H₈. The grams box is not needed. ✓
Dr. Karmach

Practice 1: moles of I₂ to kilojoules

H₂(g) + I₂(s) → 2 HI(g) · ΔH = +53.0 kJ
given: 2.50 mol I₂ · wanted: ΔH in kJ

What is ΔH, in kJ, when 2.50 mol of I₂ reacts?

  1. +66.3
  2. −133
  3. +133
  4. +0.0472
Dr. Karmach

Practice 1 · answer: C

H₂(g) + I₂(s) → 2 HI(g) · ΔH = +53.0 kJ
2.50 mol I₂ · +53.0 kJ per 1 mol I₂
2.50 mol I₂ × +53.0 kJ1 mol I₂ = +133 kJ (answer C)

A put HI's coefficient under ΔH: 2.50 × 53.0 ÷ 2 = +66.3 kJ, but I₂'s coefficient is 1. B gave the sign of a release: ΔH is positive, so heat is absorbed. D flipped the factor: 2.50 ÷ 53.0 = 0.0472, and mol never cancels.

Each mole of I₂ absorbs 53.0 kJ, and 2.50 mol absorbs 2.5 times that: about 130 kJ. ✓
Dr. Karmach

Practice 2: moles of NH₃ to kilojoules

N₂(g) + 3 H₂(g) → 2 NH₃(g) · ΔH = −92.2 kJ
given: 3.60 mol NH₃ formed · wanted: ΔH in kJ

What is ΔH, in kJ, when 3.60 mol of NH₃ forms?

  1. −111
  2. −166
  3. −0.0781
  4. −332
Dr. Karmach

Practice 2 · answer: B

N₂(g) + 3 H₂(g) → 2 NH₃(g) · ΔH = −92.2 kJ
3.60 mol NH₃ · −92.2 kJ per 2 mol NH₃
3.60 mol NH₃ × −92.2 kJ2 mol NH₃ = −166 kJ (answer B)

D kept −92.2 kJ per 1 mol NH₃: 3.60 × −92.2 = −332 kJ, double the answer, because the equation forms 2 mol. A put H₂'s coefficient under ΔH: 3.60 × −92.2 ÷ 3 = −111 kJ. C flipped the factor: 3.60 × 2 ÷ −92.2 = −0.0781, and mol never cancels.

Per mole of NH₃ the heat is −92.2 ÷ 2 = −46.1 kJ, and 3.60 mol × 46 kJ is near 166 kJ released. ✓
Dr. Karmach

Worked example 3: grams of fuel to kilojoules

CH₄(g) + 2 O₂(g) → CO₂(g) + 2 H₂O(l) · ΔH = −890 kJ
given: 40.0 g CH₄ burned · molar mass CH₄ = 16.04 g/mol · wanted: ΔH

Burn 40.0 g of methane completely. What is ΔH for this amount of fuel?

Two conversion factors are needed: grams to moles, then moles to kilojoules.

Dr. Karmach

Worked example 3: solution

CH₄(g) + 2 O₂(g) → CO₂(g) + 2 H₂O(l) · ΔH = −890 kJ
40.0 g CH₄ · 16.04 g/mol · −890 kJ per 1 mol CH₄

Two conversion factors are needed.

Step 1 · Pick the ΔH orientation

Two orientations exist. Only the one canceling mol CH₄ is used: −890 kJ / 1 mol CH₄, not 1 mol CH₄ / −890 kJ.

Dr. Karmach

Worked example 3: solution

CH₄(g) + 2 O₂(g) → CO₂(g) + 2 H₂O(l) · ΔH = −890 kJ
40.0 g CH₄ · 16.04 g/mol · −890 kJ per 1 mol CH₄
Two conversion factors are needed. Step 1 · Pick the ΔH orientation Step 2 · Chain grams → moles → kilojoules
40.0 g × 1 mol16.04 g × −890 kJ1 mol = −2220 kJ
40.0 g is about 2.5 mol, each releasing 890 kJ: ΔH ≈ −2220 kJ, about 2200 kJ given off. ✓
Dr. Karmach

Worked example 3: the route on the map

CH₄(g) + 2 O₂(g) → CO₂(g) + 2 H₂O(l) · ΔH = −890 kJ
given: 40.0 g CH₄ · found: −2220 kJ

Grams in hand: two arrows, two conversion factors. Molar mass first, then ΔH per mole of CH₄. ✓
Dr. Karmach

Worked example 4: when the coefficient is 2

2 SO₂(g) + O₂(g) → 2 SO₃(g) · ΔH = −198.2 kJ
given: 87.9 g SO₂ · molar mass SO₂ = 64.07 g/mol · wanted: heat evolved in kJ

Calculate the heat evolved when 87.9 g of sulfur dioxide is converted to sulfur trioxide.

Same grams → moles → kilojoules chain as the methane problem. SO₂'s coefficient is 2, and that 2 goes under ΔH.

Dr. Karmach

Worked example 4: solution

2 SO₂(g) + O₂(g) → 2 SO₃(g) · ΔH = −198.2 kJ
87.9 g SO₂ · 64.07 g/mol · −198.2 kJ per 2 mol SO₂

Step 1 · Write ΔH per mole of SO₂

−198.2 kJ is the heat for the equation as written, which burns 2 mol of SO₂. Per mole of SO₂ that is −198.2/2 = −99.1 kJ. Keeping −198.2 per mole doubles the answer to −272 kJ: wrong.

Dr. Karmach

Worked example 4: solution

2 SO₂(g) + O₂(g) → 2 SO₃(g) · ΔH = −198.2 kJ
87.9 g SO₂ · 64.07 g/mol · −198.2 kJ per 2 mol SO₂
Step 1 · Write ΔH per mole of SO₂ Step 2 · Chain grams → moles → kilojoules
87.9 g × 1 mol SO₂64.07 g × −198.2 kJ2 mol SO₂ = −136 kJ
87.9 g is about 1.4 mol of SO₂, each releasing about 99 kJ: near −140 kJ. ✓
Dr. Karmach

Worked example 4: the route on the map

2 SO₂(g) + O₂(g) → 2 SO₃(g) · ΔH = −198.2 kJ
given: 87.9 g SO₂ · found: −136 kJ

The same two arrows as the methane route. Only the ΔH factor changes: −198.2 kJ per 2 mol SO₂. ✓
Dr. Karmach

Take-home: divide by the coefficient

−198.2 kJ per 2 mol SO₂ = −99.1 kJ per 1 mol SO₂
the kJ-per-mole factor for any species: ΔH over that species' coefficient

ΔH belongs to the whole equation, not to any one substance. The conversion factor puts the species' coefficient under ΔH. A coefficient of 1 hides the division; a 2 does not.

Dr. Karmach

Where this goes wrong

from H₂ + ½ O₂ → H₂O(l), ΔH = −286 kJ, find 2 H₂O(l) → 2 H₂ + O₂
correct: reverse and double → ΔH = +572 kJ
Forgetting to flip the sign. Scaling but keeping the original sign gives −572 kJ. The target is the reverse, so the sign must flip: +572 kJ.
Forgetting to scale. Flipping the sign but leaving the coefficients out gives +286 kJ. Every coefficient doubled, so ΔH doubles: +572 kJ.
Leaving ΔH unchanged. Copying −286 kJ ignores both moves. The equation was reversed and doubled; ΔH must be too.
Dr. Karmach

Practice 3

N₂(g) + O₂(g) → 2 NO(g) · ΔH = +180 kJ
given: this equation and ΔH · wanted: ΔH for 4 NO(g) → 2 N₂(g) + 2 O₂(g)

What is ΔH, in kJ, for 4 NO(g) → 2 N₂(g) + 2 O₂(g)?

  1. +360
  2. −360
  3. −180
  4. +180
Dr. Karmach

Practice 3 · answer: B

N₂(g) + O₂(g) → 2 NO(g) · ΔH = +180 kJ
target: 4 NO → 2 N₂ + 2 O₂ · reversed and ×2
ΔH = −(2 × 180 kJ) = −360 kJ (answer B)

A scaled but kept the sign: 2 × 180 = +360 kJ. C flipped the sign but did not scale: −180 kJ. D left ΔH untouched at +180 kJ.

Forming 2 mol NO absorbed 180 kJ, so making 4 mol the reverse way releases twice that: −360 kJ. ✓
Dr. Karmach

Practice 4: grams of H₂ to kilojoules

2 H₂(g) + O₂(g) → 2 H₂O(l) · ΔH = −572 kJ
given: 1.00 g H₂ burned · wanted: ΔH in kJ

A balloon holds 1.00 g of hydrogen gas. What is ΔH, in kJ, when it burns completely?

  1. −284
  2. +142
  3. 0.496
  4. −142
Dr. Karmach

Practice 4 · answer: D

2 H₂(g) + O₂(g) → 2 H₂O(l) · ΔH = −572 kJ
1.00 g H₂ · 2.016 g/mol · −572 kJ per 2 mol H₂
1.00 g × 1 mol H₂2.016 g × −572 kJ2 mol H₂ = −142 kJ (answer D)

A kept −572 kJ per 1 mol H₂: 0.496 × −572 = −284 kJ, double the answer, because the equation burns 2 mol. B dropped the sign: burning releases heat, so ΔH is negative. C stopped at moles: 1.00 ÷ 2.016 = 0.496 mol, one factor short of kilojoules.

1.00 g is about half a mole of H₂, and each mole releases 286 kJ: about 143 kJ released. ✓
Dr. Karmach

Practice 5

2 Mg(s) + O₂(g) → 2 MgO(s) · ΔH = −1203 kJ
given: 2.50 × 10² kJ released · molar mass Mg 24.31 g/mol · wanted: g Mg

A magnesium flare burns white-hot. What mass of magnesium, in grams, must burn to release 2.50 × 10² kJ?

  1. 10.1
  2. 5.05
  3. 0.416
  4. 0.0171
Dr. Karmach

Practice 5 · answer: A

2 Mg(s) + O₂(g) → 2 MgO(s) · ΔH = −1203 kJ
2.50 × 10² kJ released · 1203 kJ per 2 mol Mg · Mg = 24.31 g/mol
2.50 × 10² kJ × 2 mol Mg1203 kJ × 24.31 g Mg1 mol Mg = 10.1 g Mg (answer A)

B kept 1203 kJ per 1 mol Mg: 2.50 × 10² ÷ 1203 × 24.31 = 5.05 g, half the true mass, because the equation burns 2 mol. C stopped at moles: 2.50 × 10² × 2/1203 = 0.416 mol Mg, one factor short of grams. D divided by the molar mass instead of multiplying: 0.416 ÷ 24.31 = 0.0171 g.

One mole of Mg releases about 600 kJ, so 250 kJ takes about 0.4 mol, near 10 g at 24 g each. ✓
Dr. Karmach

Practice 5: the route on the map

2 Mg(s) + O₂(g) → 2 MgO(s) · ΔH = −1203 kJ
given: 2.50 × 10² kJ released · found: 10.1 g Mg

The route runs backward. Kilojoules to moles uses ΔH written 2 mol Mg over 1203 kJ; moles to grams uses molar mass. ✓
Dr. Karmach

Practice 6

2 C₈H₁₈(l) + 25 O₂(g) → 16 CO₂(g) + 18 H₂O(l) · ΔH = −10,941 kJ
given: 35.0 g octane burned · molar mass C₈H₁₈ = 114.22 g/mol · wanted: ΔH in kJ, sign included

A lawn-mower engine burns 35.0 g of octane. What is ΔH, in kJ, for burning this amount?

  1. −5.60 × 10⁻⁵
  2. 0.306
  3. +1.68 × 10³
  4. −1.68 × 10³
  5. −3.35 × 10³
Dr. Karmach

Practice 6 · answer: D

2 C₈H₁₈(l) + 25 O₂(g) → 16 CO₂(g) + 18 H₂O(l) · ΔH = −10,941 kJ
35.0 g C₈H₁₈ · 114.22 g/mol · −10,941 kJ per 2 mol C₈H₁₈
35.0 g × 1 mol C₈H₁₈114.22 g × −10,941 kJ2 mol C₈H₁₈ = −1.68 × 10³ kJ (answer D)

A flipped the ΔH factor: 0.306 mol × (2 mol / −10,941 kJ) = −5.60 × 10⁻⁵, and mol never cancels. B stopped at moles: 35.0 ÷ 114.22 = 0.306 mol, one factor short of kilojoules. C dropped the sign: combustion releases heat, so ΔH is negative. E used −10,941 kJ per 1 mol: 0.306 × (−10,941) = −3.35 × 10³ kJ, double the answer, because the equation burns 2 mol.

Per mole of octane the heat is −10,941 ÷ 2 = −5470.5 kJ, and 0.306 mol is under a third of a mole: about 1680 kJ released. ✓
Dr. Karmach

Check yourself

  1. An equation is reversed and its coefficients tripled. What two changes apply to ΔH?
  2. A reaction releases 500 kJ per mole. Write the conversion factor that turns moles of it into kilojoules, and state which unit cancels.

The kJ-per-mole factor returns with melting and boiling. A heat of fusion or vaporization in kJ/mol turns moles of a substance into kilojoules, along the same grams → moles → kilojoules route.

Dr. Karmach

Can you…?

  • ☐ tell kinetic from potential energy and convert energy among joules, calories, kilojoules, and food Calories?
  • ☐ classify a process as exothermic or endothermic from the sign of ΔH, a heat term in the equation, or what is observed?
  • ☐ use q = m·c·ΔT to find heat, mass, specific heat, or temperature change, and compare how specific heats set the temperature response to the same heat?
  • ☐ apply heat lost = heat gained in a coffee-cup calorimeter to find the heat change of a metal, its specific heat, or the heat of a reaction in solution?
  • ☐ find the energy content of a food from the water's temperature rise in a bomb calorimeter, in kJ and Calories per gram?
  • ☐ write a thermochemical equation and use ΔH as a conversion factor for moles or grams of any substance in it?

If any box stays empty, the practice site has a drill for it. 🧪

Dr. Karmach

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